6310-31-2

Basic information

• Product Name: S-(4-chlorophenyl) 4-chlorobenzenecarbothioate
• CAS NO: 6310-31-2
• Molecular Formula: C₁₃H₈Cl₂OS
• Molecular Weight: 283.173
• Mol File: 6310-31-2.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 388.3°C at 760 mmHg
• Flash Point: 188.6°C
• Density: 1.41g/cm³
• Vapor Pressure: 3.1E-06mmHg at 25°C
• Refractive Index: 1.66
• CAS DataBase Reference: S-(4-chlorophenyl) 4-chlorobenzenecarbothioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-(4-chlorophenyl) 4-chlorobenzenecarbothioate(6310-31-2)
• EPA Substance Registry System: S-(4-chlorophenyl) 4-chlorobenzenecarbothioate(6310-31-2)

Safety Data

• Hazardous Substances Data: 6310-31-2(Hazardous Substances Data)

Upstream product

• 122-01-0 4-chloro-benzoyl chloride 
• 106-54-7 p-Chlorothiophenol 
• 637-87-6 1-Chloro-4-iodobenzene 
• 104-88-1 4-chlorobenzaldehyde 
• 7099-88-9 4-chlorophenylglyoxylic acid 
• 1195-44-4 4-chlorobenzyl methyl ether 
• 106-43-4 para-chlorotoluene 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 

Downstream Products

• 32792-53-3 4-cyanophenyl 4-chlorobenzoate 
• 39153-42-9 p-Chlor-dithiobenzoesaeure-p-chlorphenylester 
• 6833-15-4 4-chlorobenzanilide 
• 4018-82-0 4-chloro-N-(4-methoxyphenyl)benzamide 
• 39193-06-1 4,4'-dichlorobenzanilide 
• 2447-95-2 4-chloro-N-(4-tolyl)benzamide 

Relevant articles and documents

Method for preparing benzoic acid-S-phenyl ester compound through cuprous catalysis

The invention discloses a method for preparing a benzoic acid-S-phenyl ester compound shown as a formula (IV) through cuprous catalysis. The preparation method comprises the following steps of: preparing a reaction product from a benzaldehyde compound shown as a formula (I), elemental sulfur shown as a formula (II) and an iodobenzene compound shown as a formula (III) by using cuprous iodide as a catalyst, tetraethylammonium bromide as an alkali and N, N-dimethylformamide as a medium, and carrying out post-treatment on the reaction product to obtain the benzoic acid-S-phenyl ester compound, wherein the formulas are described in the specification. The method is efficient in chemical agent and low in cost; and the catalytic system has wide adaptability and is suitable for large-scale production of chemical intermediates.

Direct oxidative coupling of thiols and benzylic ethers via C(sp3)-H activation and C-O cleavage to lead thioesters

An unprecedented C-S formation method via direct oxidative C(sp3)-H bond functionalization and C-O cleavage of benzylic ethers was developed. Various thioesters including thioester structure containing drug intermediates could be achieved by th

Iron-catalyzed synthesis of thioesters from thiols and aldehydes in water

The preparation of thioesters through the iron-catalyzed coupling reaction of thiols with aldehydes is described. The reactions were carried out by using tert-butyl hydroperoxide (TBHP) as an oxidant and water as a solvent in most cases. This system is co