Tag: M.W=150-200

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 1878-65-5, formula is C8H7ClO2, Name is 3-Chlorophenylacetic acid. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. COA of Formula: C8H7ClO2.

Shao, Wen;Besnard, Celine;Guenee, Laure;Mazet, Clement research published 《 Ni-Catalyzed Regiodivergent and Stereoselective Hydroalkylation of Acyclic Branched Dienes with Unstabilized C(sp³) Nucleophiles》, the research content is summarized as follows. Two complementary regiodivergent [(P,N)Ni]-catalyzed hydroalkylations of branched dienes are reported. When amides are employed as unstabilized C(sp³) nucleophiles, a highly regioselective 1,4-addition process is favored. The addition products are obtained in high yield and with excellent stereocontrol of the internal olefin. With use of a chiral ligand and imides as carbon nucleophiles, a 3,4-addition protocol was developed, enabling construction of two contiguous tertiary stereocenters in a single step with moderate to high levels of diastereocontrol and excellent enantiocontrol. Both methods operate under mild reaction conditions, display a broad scope, and show excellent functional group tolerance. The synthetic potential of the 3,4-hydroalkylation reaction was established via a series of postcatalytic modifications.

COA of Formula: C8H7ClO2, 3-Chlorophenylacetic acid is a useful research compound. Its molecular formula is C8H7ClO2 and its molecular weight is 170.59 g/mol. The purity is usually 95%.
3-Chlorophenyl acetic acid is a compound that has resonance mass of 269. The compound reacts with HBr and water to produce 3-chlorobenzene, carbon dioxide and hydrogen chloride. A reaction product of this chemical is covid-19 pandemic (a type of drug)., 1878-65-5.

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

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Related Products of 6334-18-5.

Shekarlab, Nayereh;Ghorbani-Vaghei, Ramin;Alavinia, Sedigheh research published 《 Preparation and characterization of copper/polysulfonamide complex immobilized on graphene oxide as a novel catalyst for the synthesis of pyrimido[1,2-a]benzimidazoles》, the research content is summarized as follows. Copper-polysulfonamide complex immobilized on graphene oxide as a novel heterogeneous catalyst (GO@PSA-Cu) was synthesized and the structure and morphol. of catalyst were characterized with various anal. techniques such as Fourier-transform IR spectroscopy, SEM, energy-dispersive X-ray, N₂ isotherms, elemental mapping, inductively coupled plasma-MS, and thermogravimetric anal. The GO@PSA-Cu catalyst demonstrated good to excellent yields for the synthesis new derivatives of pyrimido[1,2-a]benzimidazoles I (R = 2-OMe, 4-Cl, 2.3-di-Cl, etc.) via one-pot three-component condensation reaction of various aromatic aldehydes, 2-aminobenzimidazole, and Et acetoacetate in ethanol. The method presented herein has several prominent advantages such as cost-effectiveness, operational simplicity, short reaction times, high yields, and reusability of the catalyst even after six consecutive runs.

Related Products 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. 3900-89-8, formula is C6H6BClO2, Name is (2-Chlorophenyl)boronic acid. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Electric Literature of 3900-89-8.

Shen, Dadong;Liu, Hanyu;Qian, Feng;Wang, Pu research published 《 Design, synthesis and evaluation of novel thienopyridazine derivatives as Chk1/2 inhibitors》, the research content is summarized as follows. In order to search for novel checkpoint kinase 1/2 (Chk1) inhibitors, a series of new compounds I.HCl [X = H₂C, HN; R = 4-MeO, 4-Cl, 3-Cl, etc.; R₁ = pyrrolidin-3-ylmethyl, 3-piperidylmethyl, 3-piperidyl, (3S)-3-piperidyl, 4-piperidyl; R₂ = H, Me, Et, etc.] and II [X = H₂C, HN; R = 4-MeO, 4-Cl, 3-Cl, etc.; R₂ = H, Me, Et, etc.; R₃ = (1-tert-butoxycarbonylpyrrolidin-3-yl)methyl, (1-tert-butoxycarbonyl-3-piperidyl)methyl, 1-tert-butoxycarbonylazetidin-3-yl, etc.] incorporating thienopyridazine core were designed and synthesized. Bioevaluation showed that compounds I.HCl [X = HN, R = 3-Cl, R₁ = 3-piperidylmethyl, R₂ = Et; X = HN, R = 2-Cl, R₁ = pyrrolidin-3-ylmethyl, R₂ = Et; X = H₂C, R = 4-Cl, R₁ = 3-piperidyl, R₂ = Me; X = HN, R = 3-F, R₁ = (3S)-3-piperidyl, R₂ = H] exhibited relatively good inhibitory activity. Notably, compound I.HCl [X = HN, R = 3-F, R₁ = (3S)-3-piperidyl, R₂ = H] displayed high selectivity against a panel of kinases and inhibited Chk1/2 signaling pathway stimulated by DNA damage drugs in cellular level. Mol. docking of I.HCl [X = HN, R = 3-F, R₁ = (3S)-3-piperidyl, R₂ = H] to the ATP-binding site of Chk1 kinase domain indicated the existence of polar interactions between I.HCl [X = HN, R = 3-F, R₁ = (3S)-3-piperidyl, R₂ = H] and the ATP-ribose-binding residues of Chk1. In mouse HT-29 xenografts, a synergistic effect was observed Co-treatment by CPT-11 and I.HCl [X = HN, R = 3-F, R₁ = (3S)-3-piperidyl, R₂ = H] significantly diminished the tumor volume, indicating the great potential of I.HCl [X = HN, R = 3-F, R₁ = (3S)-3-piperidyl, R₂ = H] as a candidate of Chk1/2 inhibitor.

Electric Literature of 3900-89-8, 2-Chlorophenylboronic acid is a useful research compound. Its molecular formula is C6H6BClO2 and its molecular weight is 156.38 g/mol. The purity is usually 95%.
2-Chlorophenylboronic acid used in the preparation of imidazo[1,2-a]pyridine amides which has tuberculostatic activity.
2-Chlorophenylboronic acid is a diphenyl ether that can be used as a building block for the synthesis of benzodiazepine receptor ligands. It has been shown to be an efficient nucleophile, leading to the formation of carbonyl groups in the presence of halides. 2-Chlorophenylboronic acid has also been shown to inhibit p38 kinase activity and may be useful for anticancer therapy., 3900-89-8.

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

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 1878-65-5, formula is C8H7ClO2, Name is 3-Chlorophenylacetic acid. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Formula: C8H7ClO2.

Shi, Xiufang;Yu, Zhenqiang;Zhu, Chaoran;Jiang, Linlin;Geng, Nanqi;Fan, Xingting;Guan, Zhanghui;Lu, Xiang research published 《 Synthesis and structure-activity relationships of pirfenidone derivatives as anti-fibrosis agents in vitro》, the research content is summarized as follows. Pirfenidone (PFD) was the first approved drug by FDA for the treatment of idiopathic pulmonary fibrosis (IPF). However, the rapid metabolism of 5-Me of PFD increases the risk of side effects in clinics. Thus, in this paper, a common practice that a stable amide bond linking various groups used to replace 5-Me of PFD in medicinal chem. was applied, and total 18 PFD derivatives were synthesized. All compounds were investigated for their antiproliferation activities against NIH3T3 cells and the structure-activity relationships of the target compounds were also discussed. Among them, YZQ17 possessed potent antiproliferation activity compared to PFD and better potency in inhibiting TGF-β-induced migration of NIH3T3 cells at a much lower concentration than that of PFD. In addition, YZQ17 dramatically inhibited the expression levels of fibrotic markers α-SMA, collagen I, and fibronectin. Moreover, further mechanistic studies confirmed that YZQ17 exhibited this considerable anti-fibrosis activity via the TGF-β/Smad2/3 dependent pathway. Finally, the results of human and rat liver microsomes assay in vitro and pharmacokinetic assay in rats confirmed that YZQ17 showed better pharmacokinetics than that of PFD. Collectively, the preliminary study of PFD derivatives modified by the amide group indicated that YZQ17 could be regarded as a lead compound for further investigation and optimization.

1878-65-5, 3-Chlorophenylacetic acid is a useful research compound. Its molecular formula is C8H7ClO2 and its molecular weight is 170.59 g/mol. The purity is usually 95%.
3-Chlorophenyl acetic acid is a compound that has resonance mass of 269. The compound reacts with HBr and water to produce 3-chlorobenzene, carbon dioxide and hydrogen chloride. A reaction product of this chemical is covid-19 pandemic (a type of drug)., Formula: C8H7ClO2

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

Chlorinated organic compounds are found in nearly every class of biomolecules. 3900-89-8, formula is C6H6BClO2, Name is (2-Chlorophenyl)boronic acid. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Name: (2-Chlorophenyl)boronic acid.

Shi, Zhaojiang;Lu, Hao-Kuan;Li, Nan;Yuan, Yaofeng;Li, Zhen;Ye, Ke-Yin research published 《 Electrochemical oxidative dearomatization of 2-arylthiophenes》, the research content is summarized as follows. A green and sustainable electrochem. oxidative dearomatization of 2-arylthiophenes was reported. The variation of substitution patterns afforded easy access to both C2/C3 and C2/C5 difunctionalized dearomative dihydrothiophenes such as I [R = Ph, 3-FC₆H₄, 2-pyridyl, etc.; R¹ = OAc, OC(O)Et]. The synthetic utility of the resulting dihydrothiophenes was further demonstrated by the concise synthesis of a pyridazinone analog with interesting vasodilator activity.

3900-89-8, 2-Chlorophenylboronic acid is a useful research compound. Its molecular formula is C6H6BClO2 and its molecular weight is 156.38 g/mol. The purity is usually 95%.
2-Chlorophenylboronic acid used in the preparation of imidazo[1,2-a]pyridine amides which has tuberculostatic activity.
2-Chlorophenylboronic acid is a diphenyl ether that can be used as a building block for the synthesis of benzodiazepine receptor ligands. It has been shown to be an efficient nucleophile, leading to the formation of carbonyl groups in the presence of halides. 2-Chlorophenylboronic acid has also been shown to inhibit p38 kinase activity and may be useful for anticancer therapy., Name: (2-Chlorophenyl)boronic acid

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

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Recommanded Product: 2,3-Dichlorobenzaldehyde.

Shinde, Rahul A.;Adole, Vishnu A.;Jagdale, Bapu S.;Desale, Bhatu S. research published 《 Synthesis, antibacterial and computational studies of Halo Chalcone hybrids from 1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)ethan-1-one》, the research content is summarized as follows. In an endeavor to develop antibacterial agents, a series of six 1,4-benzodioxan-6-yl substituted chalcone derivatives were synthesized by the base-catalyzed Claisen-Schmidt reaction of the 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)ethan-1-one with fluoro and chloro substituted aromatic aldehydes. The synthesized products were characterized by FT-IR, ¹H NMR, and ¹³C NMR spectroscopic techniques. The d. functional theory (DFT) calculations were performed using the B3LYP functional with the 6-31G(d,p) basis set for the optimization of mol. geometries and frequency calculations The CAM-B3LYP functional with a 6-31G(d,p) basis set was used in time-dependent d. functional theory (TD-DFT) calculations for the electronic absorption studies. Optimized geometries, frontier MO_s,Claisen-Schmidt condensation, and global reactivity descriptors’ specifications were computed and addressed. The simulated electronic absorption spectra were recorded in the gas phase and dichloromethane (DCM) solvent. The electronic configurations, oscillator strengths, and excited state energies were also discussed. The theor. UV-Vis and IR vibrational analyses were equated with the exptl. findings for the assignment of absorption bands. The synthesized chalcones were evaluated for in vitro antibacterial activities against two Gram pos. bacteria (Bacillus subtilis and Staphylococcus aureus) and two Gram neg. bacteria (Escherichiacoli and Proteus vulgaris). The DFT simulations were correlated with the antibacterial findings and it was discovered that they were highly helpful in the designing antibacterial agents and to establish the structure-activity relationship. Theor. calculations was in good correlation with the in vitro antibacterial results.

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., Recommanded Product: 2,3-Dichlorobenzaldehyde

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. Application of C7H4Cl2O.

Shinde, Rahul A.;Adole, Vishnu A.;Jagdale, Bapu S.;Pawar, Thansing B. research published 《 Superfast synthesis, antibacterial and antifungal studies of halo-aryl and heterocyclic tagged 2,3-dihydro-1H-inden-1-one candidates》, the research content is summarized as follows. Synthesis of halo-aryl and heterocyclic labeled 2,3-dihydro-1H-inden-1-one derivatives, as well as their antibacterial and antifungal properties are described. A total of 15 derivatives from 2,3-dihydro-1H-inden-1-one I (R = 2-thienyl, 2-pyridyl, 4-FC₆H₄, etc.) were synthesized by grinding, stirring, and ultrasound irradiation methods. The findings revealed that the ultrasound technique is increasingly satisfactory in terms of time and synthetic performance. The synthesized compounds have been tested for their antimicrobial activities against two Gram-pos. (Staphylococcus aureus and Bacillus subtilis) and two Gram-neg. bacteria (Escherichia coli and Proteus vulgaris), and also two fungal agents (Aspergillus niger and Candida albicans). Most of the compounds were found to exert potent antibacterial action with broad-spectrum antibacterial activity. Likewise, few compounds were revealed to have potent antifungal properties against A. niger and C. albicans.

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

Chloride substituents modify the physical properties of organic compounds in several ways. 1878-65-5, formula is C8H7ClO2, Name is 3-Chlorophenylacetic acid. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. Category: chlorides-buliding-blocks.

Shirase, Satoru;Tamaki, Sota;Shinohara, Koichi;Hirosawa, Keishi;Tsurugi, Hayato;Satoh, Tetsuya;Mashima, Kazushi research published 《 Cerium(IV) Carboxylate Photocatalyst for Catalytic Radical Formation from Carboxylic Acids: Decarboxylative Oxygenation of Aliphatic Carboxylic Acids and Lactonization of Aromatic Carboxylic Acids》, the research content is summarized as follows. We found that in situ generated cerium(IV) carboxylate generated by mixing the precursor Ce(O^tBu)₄ with the corresponding carboxylic acids served as efficient photocatalysts for the direct formation of carboxyl radicals from carboxylic acids under blue light-emitting diodes (blue LEDs) irradiation and air, resulting in catalytic decarboxylative oxygenation of aliphatic carboxylic acids to give C-O bond-forming products such as aldehydes and ketones. Control experiments revealed that hexanuclear Ce(IV) carboxylate clusters initially formed in the reaction mixture and the ligand-to-metal charge transfer nature of the Ce(IV) carboxylate clusters was responsible for the high catalytic performance to transform the carboxylate ligands to the carboxyl radical. In addition, the Ce(IV) carboxylate cluster catalyzed direct lactonization of 2-isopropylbenzoic acid to produce the corresponding peroxy lactone and γ-lactone via intramol. 1,5-hydrogen atom transfer (1,5-HAT).

Category: chlorides-buliding-blocks, 3-Chlorophenylacetic acid is a useful research compound. Its molecular formula is C8H7ClO2 and its molecular weight is 170.59 g/mol. The purity is usually 95%.
3-Chlorophenyl acetic acid is a compound that has resonance mass of 269. The compound reacts with HBr and water to produce 3-chlorobenzene, carbon dioxide and hydrogen chloride. A reaction product of this chemical is covid-19 pandemic (a type of drug)., 1878-65-5.

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. Recommanded Product: 2,3-Dichlorobenzaldehyde.

Shivers, Grant N.;Pigge, F. Christopher research published 《 A Mild and Highly Diastereoselective Preparation of N-Alkenyl-2-Pyridones via 2-Halopyridinium Salts and Aldehydes》, the research content is summarized as follows. An exptl. simple one-pot preparation of N-alkenyl-2-pyridones I (R = 3-MeC₆H₄, 3-MeOC₆H₄, 2-pyridyl, etc.) is reported. The reaction features mild conditions using readily available 2-halopyridinium salts and aldehydes. N-Alkenyl-2-pyridone formation proceeds with high diastereoselectivity, and a wide range of aldehyde reaction partners is tolerated. Pyridone products are also amenable to further manipulation, including conversion to N-alkyl pyridones and polycyclic ring systems.

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., Recommanded Product: 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. Related Products of 6334-18-5.

Shuai, Xiaomin;Cai, Zhiqiang;Zhao, Xinyu;Chen, Yujie;Zhang, Qian;Ma, Ziwei;Hu, Junjie;Sun, Tao;Hu, Shaoqiang research published 《 A new stationary phase for capillary gas chromatography: Calix[4]resorcinarene functionalized with imidazolium cationic units》, the research content is summarized as follows. A novel calix[4]resorcinarene-based ionic liquid (C4RA-2IL) was synthesized, structurally characterized, and statically coated on capillary column as stationary phase for capillary gas chromatog. (GC). The column efficiency of the C4RA-2IL column is 3345 plates m^-1, which are determined by n-dodecane at 120°C. Based on its McReynolds constants, the C4RA-2IL column showed moderate polarity. Particularly, the C4RA-2IL column show high separation performance for a wide range of analytes and some difficult separation of meta/para-isomers. Moreover, it exhibited excellent selectivity for critical aromatic isomers of chloroaniline, bromaniline, iodoaniline, toluidine and xylidine isomers and shows advantageous separation capability over the com. polysiloxane stationary phase. This work presents a promising future of calixarene-based ionic liquid as a new type of stationary phase in GC separations

Related Products 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