71114-55-1

Basic information

• Product Name: 4-CHLORO-N-(4-CHLOROPHENYL)BENZENECARBOTHIOAMIDE
• Synonyms: 4-CHLORO-N-(4-CHLOROPHENYL)BENZENECARBOTHIOAMIDE
• CAS NO: 71114-55-1
• Molecular Formula: C₁₃H₉Cl₂NS
• Molecular Weight: 282.19
• Mol File: 71114-55-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 382.1°Cat760mmHg
• Flash Point: 184.9°C
• Appearance: /
• Density: 1.41g/cm³
• Vapor Pressure: 4.85E-06mmHg at 25°C
• Refractive Index: 1.706
• CAS DataBase Reference: 4-CHLORO-N-(4-CHLOROPHENYL)BENZENECARBOTHIOAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLORO-N-(4-CHLOROPHENYL)BENZENECARBOTHIOAMIDE(71114-55-1)
• EPA Substance Registry System: 4-CHLORO-N-(4-CHLOROPHENYL)BENZENECARBOTHIOAMIDE(71114-55-1)

Safety Data

• Hazardous Substances Data: 71114-55-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H9Cl2NS/c14-10-3-1-9(2-4-10)13(17)16-12-7-5-11(15)6-8-12/h1-8H,(H,16,17)

Upstream product

• 74-11-3 para-chlorobenzoic acid 
• 106-47-8 4-chloro-aniline 
• 165543-78-2 4-Chloro-dithiobenzoic acid 4-bromo-phenyl ester 
• 165543-77-1 4-Chloro-dithiobenzoic acid p-tolyl ester 
• 20849-33-6 phenyl p-chlorobenzenedithiocarboxylate 
• 39153-42-9 p-Chlor-dithiobenzoesaeure-p-chlorphenylester 
• 39193-06-1 4,4'-dichlorobenzanilide 

Downstream Products

• 71114-64-2 C₁₃H₁₁Cl₂N₃ 

Relevant articles and documents

4-(4-chlorphenyl)-5-(4-chlorphenyl)-4H-1,2,4-triazole-3-amine and application thereof

The invention relates to the technical field of medicines, and particularly relates to 4-(4-chlorphenyl)-5-(4-chlorphenyl)-4h-1,2,4-triazole-3-amine and the application of 4-(4-chlorphenyl)-5-(4-chlorphenyl)-4h-1,2,4-triazole-3-amine. The invention provid

ANTIMYCOBACTERIAL THIOBENZANILIDES

A group of 30 thiobenzanilides active against Mycobacterium kansasii have been synthesized and their 1H NMR and UV spectra and RM values (TLC on silica gel impregnated with methylsilicone oil) have been measured.From the correlation between the chemical shifts of the thioamide proton in the 1H NMR spectra and the Hammett constants it can be concluded that the substituents in both aromatic rings uniformly affect the electron density of the thioamide group.The antimycobacterial activity is probably connected with local molecular parameters and can be considered to be approximately additive with respect to both parts of the molecule.