141857-53-6

Basic information

• Product Name: Benzenethiol, 2-amino-6-chloro-3-methyl-
• CAS NO: 141857-53-6
• Molecular Formula: C7H8ClNS
• Molecular Weight: 173.666
• Mol File: 141857-53-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenethiol, 2-amino-6-chloro-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenethiol, 2-amino-6-chloro-3-methyl-(141857-53-6)
• EPA Substance Registry System: Benzenethiol, 2-amino-6-chloro-3-methyl-(141857-53-6)

Safety Data

• Hazardous Substances Data: 141857-53-6(Hazardous Substances Data)

Upstream product

• 72806-61-2 1-(5-Chloro-2-methylphenyl)-2-thiourea 
• 865349-52-6 BrH*C₈H₇ClN₂S 

Downstream Products

• 141857-60-5 (8-Chloro-3,5-dimethyl-4H-benzo[1,4]thiazin-2-yl)-(4-chloro-phenyl)-methanone 
• 141857-61-6 (4-Bromo-phenyl)-(8-chloro-3,5-dimethyl-4H-benzo[1,4]thiazin-2-yl)-methanone 
• 147054-45-3 N-[3-Chloro-2-(2,4-dinitro-phenylsulfanyl)-6-methyl-phenyl]-formamide 
• 147054-46-4 4-(6-Chloro-2-formylamino-3-methyl-phenylsulfanyl)-3-nitro-benzoic acid 
• 147054-49-7 N-[3-Chloro-2-(4-methoxy-2-nitro-phenylsulfanyl)-6-methyl-phenyl]-formamide 
• 147054-47-5 N-[3-Chloro-2-(4-chloro-2-nitro-phenylsulfanyl)-6-methyl-phenyl]-formamide 
• 147054-48-6 N-[2-(4-Bromo-2-nitro-phenylsulfanyl)-3-chloro-6-methyl-phenyl]-formamide 
• 152874-12-9 N-[3-Chloro-6-methyl-2-(2-nitro-4-trifluoromethyl-phenylsulfanyl)-phenyl]-formamide 
• 488085-93-4 N-[3-chloro-2-(4,5-dichloro-2-nitro-phenylsulfanyl)-6-methyl-phenyl]-formamide 
• 488085-92-3 N-[3-chloro-2-(2-chloro-6-nitro-phenylsulfanyl)-6-methyl-phenyl]-formamide 
• 488085-88-7 3-chloro-2-(2-chloro-6-nitro-phenylsulfanyl)-6-methyl-phenylamine 
• 488085-89-8 3-chloro-2-(4,5-dichloro-2-nitro-phenylsulfanyl)-6-methyl-phenylamine 
• 147054-39-5 3-Chloro-2-(2,4-dinitro-phenylsulfanyl)-6-methyl-phenylamine 
• 147054-40-8 4-(2-Amino-6-chloro-3-methyl-phenylsulfanyl)-3-nitro-benzoic acid 

Relevant articles and documents

Synthesis and antimicrobial activity of structurally flexible heterocycles with the 1,4-thiazine heterosystem

In this work, 4H-1,4-benzothiazines were synthesized by an efficient synthetic method in a single step involving heterocyclization of substituted 2-aminobenzenethiols with β-ketoester. The structures of the synthesized compounds were confirmed by their analytical and spectral data. The synthesized compounds were evaluated for their antimicrobial activity against bacterial species; E. coli and Bacillus cereus. The synthesized compounds showed significant activity against microorganisms, which can be correlated with the privileged heterocyclic structural scaffolds.