463962-26-7

Basic information

• Product Name: thiobenzoyl 2-(5,5-dimethyl-2-thiono-1,3,2-dioxaphosphorinanyl)sulfide
• Synonyms: thiobenzoyl 2-(5,5-dimethyl-2-thiono-1,3,2-dioxaphosphorinanyl)sulfide
• CAS NO: 463962-26-7
• Molecular Weight: 318.422
• Mol File: 463962-26-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: thiobenzoyl 2-(5,5-dimethyl-2-thiono-1,3,2-dioxaphosphorinanyl)sulfide(CAS DataBase Reference)
• NIST Chemistry Reference: thiobenzoyl 2-(5,5-dimethyl-2-thiono-1,3,2-dioxaphosphorinanyl)sulfide(463962-26-7)
• EPA Substance Registry System: thiobenzoyl 2-(5,5-dimethyl-2-thiono-1,3,2-dioxaphosphorinanyl)sulfide(463962-26-7)

Safety Data

• Hazardous Substances Data: 463962-26-7(Hazardous Substances Data)

Upstream product

• 10364-94-0 1-benzoylimidazole 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 98-88-4 benzoyl chloride 
• 65-85-0 benzoic acid 
• 697-45-0 5,5-dimethyl-2-thiolo-2-thiono-1,3,2-dioxaphosphorinane 
• 157841-96-8 benzoyl 2-(5,5-dimethyl-2-thiono-1,3,2-dioxaphosphorinanyl)sulfide 

Downstream Products

• 15563-40-3 N-thiobenzoylpiperidine 
• 89861-45-0 N-hydroxy-N-methylbenzenecarbothioamide 
• 95096-14-3 N-isopropylthiobenzhydroxamic acid 
• 34733-85-2 5-phenyl-1,2,3,4-thiatriazole 
• 2227-79-4 benzenecarbothioamide 
• 636-04-4 N-Phenylbenzothioamide 
• 36926-15-5 N-(2-hydroxyethyl)benzothioamide 

Relevant articles and documents

S-Thioacyldithiophosphates in the synthesis of thiohydroxamic acids and O-thioacylhydroxylamines

S-Thioacyldithiophosphates proved to be excellent thioacylating agents. They are easily available from carboxylic acids. Due to their low reactivity towards oxygen nucleophiles and high reactivity towards nitrogen ones they found application in the synthe

New, efficient and chemoselective method of thioacylation, starting from carboxylic acids

S-Acylation of dithiophosphoric acids yields mixed anhydrides 3; they readily isomerize to O-thioacyl 4 and S-thioacyl monothiophosphates 5, which treated with the excess of dithiophosphoric acid 2 can be easily converted into thioacyl dithiophosphates 6, excellent thioacylating reagents.