Category: 6334-18-5

Chlorinated organic compounds are found in nearly every class of biomolecules. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Quality Control of 6334-18-5.

Kuremoto, Tatsuya;Sadatsune, Ren;Yasukawa, Tomohiro;Yamashita, Yasuhiro;Kobayashi, Shu research published �Machine-Assisted Preparation of a Chiral Diamine Ligand Library and In Silico Screening Using Ab Initio Structural Parameters for Heterogeneous Chiral Catalysts� the research content is summarized as follows. A ligand library containing 31 chiral diamines was synthesized using a flow-based semiautomatic reductive amination system. These ligands were evaluated in a continuous-flow asym. 1,4-addition reaction with a heterogeneous Ni catalyst. Based on the exptl. results of ab initio DFT calculations, a prediction model for enantioselectivities was successfully constructed. Furthermore, virtual screening of possible ligands was conducted to identify promising structures, which showed good enantioselectivities in experiments

6334-18-5, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., Quality Control of 6334-18-5

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. SDS of cas: 6334-18-5.

Kumar, Sunil;Choudhary, Mukesh research published ã€?Molecular docking, X-ray crystallography, Hirshfeld surface and computational studies of N-((2,3-dichlorophenyl)(ethoxy)methyl)-2-methoxy-4-nitrobenzenamineã€? the research content is summarized as follows. In this study, we report the synthesis, characterization and theor. study of an organic compound namely N-((2,3-dichlorophenyl)(ethoxy)methyl)-2-methoxy-4-nitrobenzenamine (L) as potential drug candidate against SARS-CoV-2 main protease. Structural and Hirshfeld surface anal. was carried out on the organic compound (L). The potential application was also assessed through mol. docking and 3-D visualizations of intermol. interactions with two very important crucial proteins of SARS-CoV-2 (M^Pro-7C6U & 7C6S). Mol. docking calculations exhibited high binding energy and inhibition constant of -7.4 kcal/mol and 2.413 μM with SARS-CoV-2 M^Pro. Besides this, an ADMET prediction was also studied. This study provides an alternative and viable therapeutic agent for SARS-CoV-2 virus.

SDS of cas: 6334-18-5, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., 6334-18-5.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chloride substituents modify the physical properties of organic compounds in several ways. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. Electric Literature of 6334-18-5.

Kumar, Achutha Dileep;Vivek, Hamse Kameshwar;Srinivasan, Bharath;Naveen, Shivalingegowda;Kumara, Karthik;Lokanath, Neratur Krishnappagowda;Byrappa, Kullaiah;Kumar, Kariyappa Ajay research published ã€?Design, synthesis, characterization, crystal structure, Hirshfeld surface analysis, DFT calculations, anticancer, angiogenic properties of new pyrazole carboxamide derivativesã€? the research content is summarized as follows. The present study demonstrated the utility of a reverse ligand similarity based approach to identify potential targets for a new series of pyrazole carboxamides I [R = H, R¹ = H, methoxy, etc.; R₂ = H, Me, fluoro, etc.] that showed a potent anticancer activities against MCF-7 cells compared to other structurally related mols. and controls. Mol. docking studies revealed that the compound I [R = R¹ = H, R₂ = fluoro] interacted very strongly with human estrogen receptor with docking score of -8.82kcal/mol. In case of hERα-LBD, it interacted very well via hydrogen bond with Thr347 with docking score of -8.19 kcal/mol and very good binding with Asp351 via both hydrogen bonding and salt bridge. These results indicated that compound I [R = R¹ = H, R₂ = fluoro] acted as better inhibitor for estrogen receptors comparable with the standard inhibitor tamoxifen. Further, ADMET studies revealed that pyrazole carboxamides I [R = H, R¹ = H, methoxy, etc.; R₂ = H, Me, fluoro, etc.] had good ADME properties as compared with the data from 95% of drugs readily available in the market. The pyrazole carboxamides I [R = H, R¹ = H, methoxy, etc.; R₂ = H, Me, fluoro, etc.] possessed three dimensional supramol. self-assembly, in which N-H···O bonds connected the mols. and build up two dimensional arrays, which were extended to 3D network through C-H···C_g and C-Cl···C_g interactions. The structure also exhibited π···π stacking interactions, which contributed to the crystal packing. The Hirshfeld surface anal. was carried out to quantify the intermol. interactions involved in the crystalline environment. The mol. geometry of the compound I [R = H, R¹ = methoxy, R² = H] by DFT method with B3LYP hybrid functional and 6-311+G(d,p) basis set. The optimized structure was in good agreement with the exptl. findings. The electrostatic potential map was plotted to understand the energy distribution and chem. reactive regions of the mol.

Electric Literature of 6334-18-5, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., 6334-18-5.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Reference of 6334-18-5.

Kulkarni, Pramod research published ã€?An efficient solvent-free synthesis of 3,4-disubstituted isoxazole-5(4H)-ones using microwave irradiationã€? the research content is summarized as follows. One-pot and three-component synthesis of 3-mehyl-4-arylmethyleneisoxazol-5(4H)-ones I [Ar = Ph, 4-MeC₆H₄, 2-ClC₆H₄, etc.] using microwave radiation under the solvent-free conditions, in the presence of potassium bromide as the catalyst was reported. The method had given the products in high yields and short reaction times with an easy work-up process. The present method provided an easy and efficient approach for the synthesis of this class of compounds, because of its clean reaction profile and operational simplicity.

Reference of 6334-18-5, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., 6334-18-5.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chlorinated organic compounds are found in nearly every class of biomolecules. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Formula: C7H4Cl2O.

Khaleghi Abbasabadi, Masoud;Azarifar, Davood research published ã€?β-Alanine-functionalized magnetic graphene oxide quantum dots: an efficient and recyclable heterogeneous basic catalyst for the synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-dione and 2,3-dihydroquinazolin-4(1H)-one derivativesã€? the research content is summarized as follows. In this research, a novel synthesis of magnetic β-alanine-functionalized-graphene oxide quantum dots Fe₃O₄@GOQDs-N-(β-alanine) as a recyclable and eco-friendly heterogeneous nanocatalyst was reported. The catalytic efficiency of these nanosheets was explored as a basic catalyst for a one-pot three-component synthesis of various 1H-pyrazolo[1,2-b]phthalazine-5,10-dione I (Ar = 2,3-dichlorophenyl, 4-methoxyphenyl, pyridin-4-yl, etc.) and 2,3-dihydroquinazolin-4(1H)-one derivatives II (R = Me, MeO, Cl; R¹ = H, Cl; R² = H, Cl; R³ = H, Me, MeO, F, Cl). The reactions proceeded smoothly under mild and green conditions to afford the respected products I and II in excellent yields. The structure of this newly fabricated catalyst was successfully confirmed by different anal. techniques such as Fourier transform IR spectroscopy, X-ray diffraction, field emission-SEM, high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy, vibrating sample magnetometry, and thermogravimetric anal. The stability and recyclability of the catalyst were examined by performing the model reaction in six consecutive runs. The recovered catalyst from the first run was directly used for the next runs with no significant loss of catalytic activity.

6334-18-5, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., Formula: C7H4Cl2O

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

The class of organic compounds having covalently a bonded chlorine atom is called organic chlorides. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Their wide structural variety and divergent chemical properties lead to a broad range of named reactions and applications. Name: 2,3-Dichlorobenzaldehyde.

Kaya Cavusoglu, Betuel;Saglik, Beguem N.;Acar Cevik, Ulviye;Osmaniye, Derya;Levent, Serkan;Oezkay, Yusuf;Kaplancikli, Zafer A. research published ã€?Design, synthesis, biological evaluation, and docking studies of some novel chalcones as selective COX-2 inhibitorsã€? the research content is summarized as follows. A new series of chalcones 4-(SO₂Me)C₆H₄C(O)CH=CHR (R = 2-FC₆H₄, 2,4-(Cl₂)C₆H₃, 2H-1,3-benzodioxol-5-yl, etc.) possessing an SO₂CH₃ COX-2 pharmacophore at the para position of the C-1 Ph ring was synthesized via the Claisen-Schmidt condensation reaction and examined for their inhibition potential against cyclooxygenase (COX) enzymes. Enzyme inhibition studies revealed that most of the compounds showed a moderate-to-strong inhibitory activity (IC₅₀ = 0.18-0.34μM) against the COX-2 enzyme as compared with celecoxib (IC₅₀ = 0.12μM), ibuprofen (IC₅₀ = 5.33μM), and nimesulide (IC₅₀ = 1.68μM). Among these compounds, 4-(SO₂Me)C₆H₄C(O)CH=CHR (R = 2,3-(Cl₂)C₆H₃; 2,4-(Cl₂)C₆H₃; 2-Cl-6-F-C₆H₃) became prominent with IC₅₀ values of 0.21, 0.19, and 0.18μM, resp. According to mol. docking studies of the most effective compounds, it was found that the compounds interact with amino acids that are important in COX-2 selectivity, such as Arg499 and Phe504.

6334-18-5, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., Name: 2,3-Dichlorobenzaldehyde

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chloride substituents modify the physical properties of organic compounds in several ways. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. Application of C7H4Cl2O.

Karimi Askarani, Hajar;Karimi Zarchi, Mohammad Ali;Mirjalili, BiBi Fatemeh;Bamoniri, Abdolhamid research published ã€?One-pot synthesis of polyhydroquinoline derivatives using nano-Fe₃O₄@dextrin/BF₃ as a magnetic biodegradable catalystã€? the research content is summarized as follows. In this study, the magnetized nano-dextrin-supported boron trifluoride (nano-Fe₃O₄@dextrin/BF₃) as a green biopolymer-based catalyst is synthesized in two steps. In the first step, nano-dextrin is magnetized (nano-Fe₃O₄@dextrin), and in the second step, the BF₃ is supported to the obtained nano-Fe₃O₄@dextrin. The structure of nano-Fe₃O₄@dextrin/BF₃ is characterized by different techniques, including Fourier transform IR (FT-IR) spectroscopy, X-ray diffraction (XRD) pattern, energy dispersive X-ray (EDX) anal., SEM (SEM) imaging, mapping, vibrating sample magnetometer (VSM), and thermogravimetric anal. (TGA/DTG). The catalytic efficiency was also investigated in the synthesis of biol. active polyhydroquinoline derivatives via Hantzsch condensation reaction of aromatic aldehydes, dimedone, Et acetoacetate, and ammonium acetate under solvent-free conditions. The structure of products was confirmed by their m.ps. (MP), FT-IR, and ¹H and ¹³C NMR (NMR) spectroscopy. This procedure enjoys advantages such as short reaction time, clean and fast work-up, and easy separation of the catalyst by an external magnet.

Application of C7H4Cl2O, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., 6334-18-5.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chlorinated organic compounds are found in nearly every class of biomolecules. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Reference of 6334-18-5.

Kang, Hyotaik;Li, Chao-Jun research published �Ruthenium(II)-catalyzed regioselective 1,6-conjugate addition of umpolung aldehydes as carbanion equivalents� the research content is summarized as follows. Umpolung aldehydes as carbanion equivalent for highly regioselective 1,6-conjugate addition reactions to unsaturated ketones, with preliminary studies of the enantioselective variant was reported. The synergy of ruthenium(II) catalyst and electron-rich, bidentate phosphine ligand is essential for the reactivity and selectivity under mild reaction conditions.

6334-18-5, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., Reference of 6334-18-5

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Formula: C7H4Cl2O.

Kalhor, Mehdi;Zarnegar, Zohre research published ã€?1-Methylimidazolium ionic liquid supported on Ni@zeolite-Y: fabrication and performance as a novel multi-functional nanocatalyst for one-pot synthesis of 2-aminothiazoles and 2-aryl benzimidazolesã€? the research content is summarized as follows. In the present study, 1-methyl-3-(3-trimethoxysilylpropyl)-1H-imidazol-3-ium chloride-supported Ni@zeolite-Y-based nanoporous materials (Ni@zeolite-Im-IL) were synthesized and their structures were confirmed using different characterization techniques such as FT-IR, FE-SEM, EDX, XRD, BET and TGA-DTG analyses. In order to synthesize this multi-functional nano-system, zeolite-NaY was modified first, with exchanged Ni2+ ions and 3-chloropropyltriethoxysilane (CPTES) as a coupling reagent and then functionalized to imidazolium chloride ionic liquid by N-methylimidazole. New multi-functional nano-material of Ni@zeolite-Im-IL demonstrated high activity in the catalytic synthesis of 2-aminothiazoles 3a-l by one-pot reaction of methylcarbonyls, thiourea and iodine at 80°C in DMSO with good to excellent yields (85-98%). Also, the catalytic synthesis of 2-aryl benzimidazoles, 6a-m was performed by the condensational reaction of o-arylendiamine and aromatic aldehydes in EtOH at room temperature with excellent yields (90-98%). Advantages of this efficient synthetic strategy include higher purity and shorter reaction time, excellent yield, easy isolation of products, the good stability, activity and feasible reusability of the metallic ionic liquid nanocatalyst. These benefits have made this method more compatible with the principles of green chem.

Formula: C7H4Cl2O, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., 6334-18-5.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chlorinated organic compounds are found in nearly every class of biomolecules. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Application In Synthesis of 6334-18-5.

Kalhor, Mehdi;Seyedzade, Zahra;Zarnegar, Zohre research published ã€?(NH₄)₂Ce(NO₃)₆/HNO₃ as a High-Performance Oxidation Catalyst for the One-Step, Solvent-Free Synthesis of Dicyano Imidazolesã€? the research content is summarized as follows. The one-pot, solvent-free methodol. for preparation of 2-aryl-4,5-dicarbonitrile-imidazoles I [R = Ph, 4-O₂NC₆H₄, 4-methyl-2-thienyl, etc.] via reaction of 2,3-diaminomaleonitrile with aromatic aldehydes in presence of cerium (IV) ammonium nitrate/nitric acid (CAN/NA) as a high-performance oxidation catalyst was reported. The salient features of described process in comparison with previous methods included one-step process, easy isolation of products, higher purity and yields, milder and cleaner conditions, short reaction time and convenient manipulation.

6334-18-5, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., Application In Synthesis of 6334-18-5

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics