Month: December 2022

A green preparation of N-chloro- and N-bromosaccharin was written by de Souza, Soraia P. L.;da Silva, Joaquim F. M.;de Mattos, Marcio C. S.. And the article was included in Synthetic Communications in 2003.Recommanded Product: 14070-51-0 This article mentions the following:

The reaction of the sodium salt of saccharin, potassium chloride or bromide and oxone in water at room temperature for 24 h produced pure N-chloro- and N-bromosaccharin in 58% and 64% yield, resp. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0Recommanded Product: 14070-51-0).

2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Recommanded Product: 14070-51-0

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

Synthesis, molecular docking and biological evaluation of quinolone derivatives as novel anticancer agents was written by Li, Jie;Zheng, Tu-cai;Jin, Yi;Xu, Jian-guo;Yu, Jian-gang;Lv, Yan-wen. And the article was included in Chemical & Pharmaceutical Bulletin in 2018.Name: 3-(Trifluoromethyl)benzene-1-sulfonyl chloride This article mentions the following:

A series of novel quinolone derivatives (8a-j) I (R¹ = 4-F, 2,4-diF; R² = 4-CH₃, 2-Cl, 2,6-diCl, 2-CF₃, 3-CF₃) were synthesized, and their anticancer activities were 1 tested in human cancer cell lines, human lung carcinoma cell (A549), human promyelocytic leukemia cell (HL-60), and human cervical cancer cell (Hela). Compound 8i I (R¹ = 2,4-diF; R² = 2-CF₃) was found to be 5-times more potent in cell- killing activity for cell Iines A549, HL-60, and Hela than the pos. control irinotecan or cisplatin, with IC₅₀ of 0.009, 0.008 and 0.010μm, resp. The docking study revealed that compound 8i might have strong interactions with the active site of DNA-topoisomerase I. In the experiment, the researchers used many compounds, for example, 3-(Trifluoromethyl)benzene-1-sulfonyl chloride (cas: 777-44-6Name: 3-(Trifluoromethyl)benzene-1-sulfonyl chloride).

3-(Trifluoromethyl)benzene-1-sulfonyl chloride (cas: 777-44-6) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Name: 3-(Trifluoromethyl)benzene-1-sulfonyl chloride

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

A Simple Method for the Determination of Pharmaceutical and Personal Care Products in Fish Tissue Based on Matrix Solid-Phase Dispersion was written by Xiao, Shouchun;Lv, Shengchen;Cheng, Zheng;Hu, Caiwei;Li, Pengxi;Nan, Fang;Liu, Xueke;Liu, Donghui;Zhou, Zhiqiang;Wang, Peng. And the article was included in Journal of Agricultural and Food Chemistry in 2021.Recommanded Product: 101-20-2 This article mentions the following:

A simple and effective pretreatment method based on matrix solid-phase dispersion was developed for the determination of pharmaceutical and personal care products (PPCPs) and their metabolites in fish by high-performance liquid chromatog. tandem mass spectrometry. The type and amount of dispersant, adsorbent, and eluting solvent were optimized by a single-factor experiment and Box-Behnken design. Under the optimal conditions with 2.5 g of Florisil as a dispersant, 500 mg of C₁₈ as an adsorbent, and 5 mL of acetonitrile as an eluting solvent, the recoveries ranged from 70.4 to 99.9% with relative standard deviations less than 10.5%, and the limits of quantitation ranged from 0.13 to 1.01μg/kg. The developed method was successfully applied to detect PPCPs in marketed fish, and five PPCPs, including triclocarban, sulfadiazine, sulfadimidine, sulfamethoxazole, and carbamazepine, were detected at trace levels. The proposed method, which has the advantages of short anal. time, less solvent consumption, and high sensitivity, can be used for the determination of trace PPCPs in fish. In the experiment, the researchers used many compounds, for example, 1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea (cas: 101-20-2Recommanded Product: 101-20-2).

1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea (cas: 101-20-2) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Recommanded Product: 101-20-2

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

Preparation of some new substituted phenylglyoxals was written by Nardi, Dante;Tajana, Alberto;Massarani, Elena. And the article was included in Annali di Chimica (Rome, Italy) in 1969.Recommanded Product: 5344-49-0 This article mentions the following:

ArCOCHO (I) are prepared by 3 different methods. II are prepared from I and o-(H2N)2C6H4; ArCOCO2H are treated with o-(H2N)2C6H4 to give III. Thus, a mixture of 15 g o-MeOC6H4Ac, 13.32 g SeO2, 50 ml HOAc, and 10 ml H2O is refluxed 5 hr to give 50% o-methoxyphenylglyoxal, b0.1 81°. Similarly prepared are the following I (Ar and b.p./mm given): o-ClC6H4, 92°/l; m-ClC6H4, 90°/1.5 (hydrate m. 82-4°); 4,2-Cl(O2N)C6H3, 118°/0.4; 5,2-Cl(O2N)C6H3, 128°/0.6; 2,4-Cl(O2N)C6H3, 118°/0.5 (hemihydrate m. 88°); 2,5-Cl(O2N)-C6H3, 137°/0.8 (hydrate m. 91-3°); 4,3-Cl(O2N)C6H3, 134°/-0.6. IV are treated with HCl to give 5,2-Cl(O2N)C6H3COCHO and 4,2-Cl(O2N)C6H3COCHO. 2-Chlor-6-nitro-ω-diazoacetophenone (0.03 mole) is treated with 0.031 mole Ph3P to give 2,6-Cl(O2N)C6H3CH:NN:PPh3, m. 182°, which (4.87 g) is treated with 1.52 g NaNO2, 18 ml 2M HCl, and 3.9 g PhNHCH2CH2NHPh to give V [Ar = 2,6-Cl(O2N)C6H3] (VI), m. 151-2°. Similarly prepared are 2,4-Cl(O2N)C6H3CH:NN:PPh3, m. 162°, and V [Ar = 2,4-Cl(O2N)C6H3], m. 145-6°. VI (2.03 g) is treated with 6 ml HCl (d. 1.18) to give 30% 2,6-Cl(O2N)C6H3-COCHO, b0.3 110°; hydrate m. 102-4°. Similarly prepared is I [Ar = 2,4-Cl(O2N)C6H3]. Also prepared are the following II and III (Ar, m.p. II, and m.p. III given): o-MeOC6H4, 110°, 230°; o-ClC6H4, 94-5°, 237°; 4,2-Cl(O2N)C6H3, 195°, 322°; 5,2-Cl(O2N)C6H3, 166-7°, 306°; 2,4-Cl(O2N)C6H3, 175°, 313°; 2,5-Cl(O2N)C6H3, 216°, 324-5°; 4,3-Cl(O2N)C6H3, 187-8°, 298°. Also the following II (Ar and m.p. given): m-ClC6H4, 130°; 2,6-Cl(O2N)C6H3, 121-2°. Also the following III (Ar and m.p. given): M-MeOC6H4, 183°; m-O2NC6H3, 328-9°; p-O2NC6H4, 350°. Also the following IV (Ar and m.p. given): m-ClC6H4, 184°; 2,4-Cl(O2N)C6H3, 231°; 5,2-Cl(O2N)C6H3, 199-201°; 4,3-Cl(O2N)C6H3, 190°. Also the following compounds: 2,6-Cl-(O2N)C6H3COCHAcCO2Et (m. 68-9°), 2,6-Cl(O2N)C6H3Ac (m. 60°), 2,6-Cl(O2N)C6H3COCH2Ac (m. 85°), 2,4-Cl(O2N)C6H3Ac 4,2-Cl(O2N)C6H3Ac. In the experiment, the researchers used many compounds, for example, 2-Chloro-6-nitrobenzoic acid (cas: 5344-49-0Recommanded Product: 5344-49-0).

2-Chloro-6-nitrobenzoic acid (cas: 5344-49-0) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Recommanded Product: 5344-49-0

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

Regioselective synthesis of vic-halo alcohols and symmetrical or unsymmetrical vic-dihalides from epoxides using triphenylphosphine-N-halo imides was written by Iranpoor, Nasser;Firouzabadi, Habib;Azadi, Roya;Ebrahimzadeh, Farzaneh. And the article was included in Canadian Journal of Chemistry in 2006.HPLC of Formula: 14070-51-0 This article mentions the following:

A simple, novel, and highly regioselective cleavage of epoxides into vicinal halo alcs. and sym. or unsym. dihalides is described using different stoichiometries of triphenylphosphine and N-halosuccinimide or N-halosaccharine (NXSac). In the experiment, the researchers used many compounds, for example, 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0HPLC of Formula: 14070-51-0).

2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.HPLC of Formula: 14070-51-0

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

Resonant two-photon ionization spectroscopy of the ³⁵Cl and ³⁷Cl isotopomers of cis and trans 3-chloro-4-fluoroanisole was written by Yu, Dan;Dong, Changwu;Zhang, Lijuan;Cheng, Min;Hu, Lili;Du, Yikui;Zhu, Qihe;Zhang, Cunhao. And the article was included in Journal of Molecular Structure in 2011.Name: 2-Chloro-1-fluoro-4-methoxybenzene This article mentions the following:

The effects of conformation and isotopic substitution on the properties of 3-chloro-4-fluoroanisole (3C4FA) were studied by mass-analyzed resonant two-photon ionization (R2PI) technique and theor. calculations In the one color R2PI spectra, the band origins of the S₁ ← S₀ electronic transitions (0⁰ bands) of cis ³⁵Cl-3C4FA and cis ³⁷Cl-3C4FA were found to be equivalent at 34,703 ± 3 cm^-1, while the 0⁰ bands of trans ³⁵Cl-3C4FA and trans ³⁷Cl-3C4FA were found to be equivalent at 34,747 ± 3 cm^-1. Assignments of the observed vibrational bands of R2PI spectra were made mainly based on the 10-electron, 8-orbital CASSCF/6-31g calculations and on conformity with the available data of the similar aromatic mols. in the literature. With the two color R2PI technique, the adiabatic ionization energies (IEs) of cis ³⁵Cl-3C4FA and cis ³⁷Cl-3C4FA were determined to be equivalently 67,349 ± 15 cm^-1, while the IEs of trans ³⁵Cl-3C4FA and trans ³⁷Cl-3C4FA were determined to be equivalently 67,595 ± 15 cm^-1. The conformational effect on the transition energies, ionization energies and vibrational frequencies of 3C4FA is greater than the isotopic effect. The hetero-dihalogen-substitution effect on the transition energies is also discussed. In the experiment, the researchers used many compounds, for example, 2-Chloro-1-fluoro-4-methoxybenzene (cas: 202925-07-3Name: 2-Chloro-1-fluoro-4-methoxybenzene).

2-Chloro-1-fluoro-4-methoxybenzene (cas: 202925-07-3) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Name: 2-Chloro-1-fluoro-4-methoxybenzene

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

Rubber manufacture: sampling and identification of volatile pollutants was written by Cocheo, Vincenzo;Bellomo, Maria Luisa;Bombi, G. Giorgio. And the article was included in American Industrial Hygiene Association Journal (1958-1999) in 1983.Application of 5335-05-7 This article mentions the following:

Air samples collected in the vulcanization and extrusion areas of a shoe-sole factory contained approx. 100 different volatile organic compounds whose concentrations ranged from 25 to 27000 μg/m³. These compounds included alkanes, cycloalkanes, aromatic hydrocarbons, chlorinated organics, phenols, esters, etc. The highest number and concentrations of pollutants were associated with the vulcanization process. In the experiment, the researchers used many compounds, for example, Chloromethyl benzoate (cas: 5335-05-7Application of 5335-05-7).

Chloromethyl benzoate (cas: 5335-05-7) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Application of 5335-05-7

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

Pyrrolobenzodiazepines with antinociceptive activity: synthesis and pharmacological activities was written by Mai, A.;Di Santo, R.;Massa, S.;Artico, M.;Pantaleoni, G. C.;Giorgi, R.;Coppolino, M. F.;Barracchini, A.. And the article was included in European Journal of Medicinal Chemistry in 1995.COA of Formula: C9H9ClO2 This article mentions the following:

The synthesis of some N-[2-(1H-pyrrol-1-yl)benzyl]arylacetamides and 4-(arylmethyl)-5,6-dihydro-4H-pyrrolo[1,2-a]-[1,4]benzodiazepines as their conformationally restricted analogs was reported. The reduction of arylacetamides and N-methylation of pyrrolobenzodiazepines led to the corresponding N-[2-(1H-pyrrol-1-yl)benzyl]arylehylamines and the 4-(arylmethyl)-5-methyl-5,6-dihydro-4H-pyrrolo[1,2-a][1,4]benzodiazepines, resp. The new compounds were subjected to pharmacol. tests for evaluation of antinociceptive effects. Neuro-behavioral assays was also carried out on selected compounds to acquire data on neurotoxicity. One of the most active compounds was 4-(4-methoxybenzyl)-5-methyl-5,6-dihydro-4H-pyrrolo[1,2-a][1,4]benzodiazepine; it showed high activity in both hot-plate and acetic-acid-induced writhing tests in mice without sedative or myorelaxant effects . In the experiment, the researchers used many compounds, for example, 2-(3-Methoxyphenyl)acetyl chloride (cas: 6834-42-0COA of Formula: C9H9ClO2).

2-(3-Methoxyphenyl)acetyl chloride (cas: 6834-42-0) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.COA of Formula: C9H9ClO2

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

Catalytic C-H Activation of Hydrocarbons by Rhodium(I) and Iridium(I) Complexes with Hemilabile Quinolyl-Cp Ligands was written by Kohl, Gerald;Rudolph, Ralph;Pritzkow, Hans;Enders, Markus. And the article was included in Organometallics in 2005.Related Products of 39722-81-1 This article mentions the following:

The rhodium(I) and iridium(I) complexes I (M = Rh, R = H 3a; M = Ir, R = H 4a; M = Rh, R = Me 5a; M = Ir, R = Me 6a) contain the hemilabile Cp-quinoline chelate ligands, where the hard nitrogen donor does not displace the good acceptor ligand ethylene. After irradiation with visible light, intensely colored complexes are obtained, where the N-donor coordinates to the metal centers. Depending on the metal atom and on the substitution pattern at the Cp rings, the mono-ethene complex with N-metal coordination can be observed spectroscopically (e.g., 3b) or C-H addition products are probable intermediates. The iridium complex 6a is able to activate the aliphatic C-H bond in cyclohexane. With the rhodium complex 5a as the precatalyst, catalytic H/D exchange reactions have been performed with olefinic substrates. With linear α-olefins a fast double-bond isomerization dominates. The hemilabile ligands stabilize the catalytically active metal complexes without suppressing their activity significantly. In the experiment, the researchers used many compounds, for example, Chlorobis(ethylene)iridium(I) dimer (cas: 39722-81-1Related Products of 39722-81-1).

Chlorobis(ethylene)iridium(I) dimer (cas: 39722-81-1) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Related Products of 39722-81-1

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

Several human cyclin-dependent kinase inhibitors, structurally related to roscovitine, as new anti-malarial agents was written by Houze, Sandrine;Hoang, Nha-Thu;Lozach, Olivier;Le Bras, Jacques;Meijer, Laurent;Galons, Herve;Demange, Luc. And the article was included in Molecules in 2014.Synthetic Route of C8H8Cl2N4 This article mentions the following:

In Africa, malaria kills one child each minute. It is also responsible for about one million deaths worldwide each year. Plasmodium falciparum, is the protozoan responsible for the most lethal form of the disease, with resistance developing against the available anti-malarial drugs. Among newly proposed anti-malaria targets, are the P. falciparum cyclin-dependent kinases (PfCDKs). There are involved in different stages of the protozoan growth and development but share high sequence homol. with human cyclin-dependent kinases (CDKs). We previously reported the synthesis of CDKs inhibitors that are structurally-related to (R)-roscovitine, a 2,6,9-trisubstituted purine, and they showed activity against neuronal diseases and cancers. In this report, we describe the synthesis and the characterization of new CDK inhibitors, active in reducing the in vitro growth of P. falciparum (3D7 and 7G8 strains). Six compounds are more potent inhibitors than roscovitine, and three exhibited IC50 values close to 1 μM for both 3D7 and 7G8 strains. Although, such mols. do inhibit P. falciparum growth, they require further studies to improve their selectivity for PfCDKs. In the experiment, the researchers used many compounds, for example, 2,6-Dichloro-9-isopropyl-9H-purine (cas: 203436-45-7Synthetic Route of C8H8Cl2N4).

2,6-Dichloro-9-isopropyl-9H-purine (cas: 203436-45-7) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Synthetic Route of C8H8Cl2N4

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