52322-79-9

Basic information

• Product Name: Benzenecarbothioic acid, 4-methyl-, O-phenyl ester
• CAS NO: 52322-79-9
• Molecular Formula: C14H12OS
• Molecular Weight: 228.315
• Mol File: 52322-79-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenecarbothioic acid, 4-methyl-, O-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarbothioic acid, 4-methyl-, O-phenyl ester(52322-79-9)
• EPA Substance Registry System: Benzenecarbothioic acid, 4-methyl-, O-phenyl ester(52322-79-9)

Safety Data

• Hazardous Substances Data: 52322-79-9(Hazardous Substances Data)

Upstream product

• 60410-77-7 bis(4-methylbenzenethiocarbonyl) sulphide 
• 139-02-6 sodium phenoxide 
• 97270-52-5 4-(methyl)thiobenzoyl diphenylthiophosphinoyl sulfide 
• 120449-42-5 Se-phenyl 4-methylbenzenecarboselenothioate 

Downstream Products

• 3481-62-7 1-<4-(methyl)thiobenzoyl>piperidine 

Relevant articles and documents

Compound embodiments that release H2S by reaction with a reactive compound and methods of making and using the same

Disclosed herein are embodiments of a donor compound that releases H2S by reacting with a reactive compound. The donor compound embodiments described herein can be used to deliver H2S to a subject or a sample and further can be used to administer therapeutic agents. The donor compound embodiments also can facilitate bioconjugation. Methods of making and using the donor compound embodiments also are disclosed.

Preparation and Some Reactions of Thioacyl Diphenylthiophosphinoyl and Thioacyl Diphenylphosphino Sulfides

The reaction of sodium or caesium dithiocarboxylates with diphenylthiophosphinic and diphenylselenophosphinic chlorides gives purple thioacyl diphenylthiophosphinoyl 5 and dark green thioacyl diphenylselenophosphinoyl sulfides 6, which are useful thioacylating reagents under mild reaction conditions.Thioacyl diphenylphosphino sulfides 22, which can be obtained by the similar method using diphenylphosphinous chlorides, react with methanol to yield the corresponding methyl dithiocarboxylates 15, while the reactions of 22 with N-chlorosuccinimide lead to hitherto unknown N-(thioacetylthio)succinimides 28.