75000-10-1

Basic information

• Product Name: 4-phenyl-5-thioxo-3-isothiazolin-3-yl S-thiobenzoate
• Synonyms: 4-phenyl-5-thioxo-3-isothiazolin-3-yl S-thiobenzoate
• CAS NO: 75000-10-1
• Molecular Weight: 329.467
• Mol File: 75000-10-1.mol

Chemical Properties

• CAS DataBase Reference: 4-phenyl-5-thioxo-3-isothiazolin-3-yl S-thiobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenyl-5-thioxo-3-isothiazolin-3-yl S-thiobenzoate(75000-10-1)
• EPA Substance Registry System: 4-phenyl-5-thioxo-3-isothiazolin-3-yl S-thiobenzoate(75000-10-1)

Safety Data

• Hazardous Substances Data: 75000-10-1(Hazardous Substances Data)

Upstream product

• 75000-14-5 5,5'-dithiobis-(4-phenyl-3-isothiazol-3-yl) O-thiobenzoate 
• 98-88-4 benzoyl chloride 
• 75564-10-2 3-mercapto-4-phenyl-3-isothiazoline-5-thione 

Downstream Products

• 78522-21-1 4-(4-Phenyl-3-thiobenzoyloxy-isothiazol-5-ylsulfanylcarbonyl)-benzoic acid methyl ester 
• 76277-83-3 5-methylthio-4-phenyl-3-thiobenzoyloxyisothiazole 1-oxide 
• 76277-72-0 N-benzoyl-<4,5-bis(methoxycarbonyl)-1,3-dithiol-2-ylidene>phenylethanethioamide 
• 75000-14-5 5,5'-dithiobis-(4-phenyl-3-isothiazol-3-yl) O-thiobenzoate 
• 78522-34-6 4-phenylisothiazol-3-yl O-thiobenzoate 
• 78522-22-2 Thiobenzoic acid O-(5-acetylsulfanyl-4-phenyl-isothiazol-3-yl) ester 
• 75000-12-3 5-ethylthio-4-phenyl-3-thiobenzoyloxyisothiazole 
• 75000-07-6 5-methylthio-4-phenyl-3-thiobenzoyloxyisothiazole 

Relevant articles and documents

Studies on Heterocyclic Chemistry. Part 24. Syntheses of the 4-Arylisothiazol-3-yl O-Thioesters utilising the S-Thioester --> O-Thioester Rearrangements of the 4-Aryl-5-thioxo-3-isothiazolin-3-yl S-Thioesters induced by Acylation Reagents, Peracid, or N-B

A number of 4-arylisothiazol-3-yl O-thioesters have been prepared utilising the S-thioester -> O-thioester rearrangements of the 4-aryl-5-thioxo-3-isothiazolin-3-yl S-thioesters (1).Reactions of the isothiazolines with acylation reagents (e.g. acyl chlori

Studies on Heterocyclic Chemistry. Part 21. Reactions of 3-Mercapto- and 3-Acylthio-3-isothiazoline-5-thiones: Ring Transformations, a Base-induced Ring Cleavage, and Thiol-ester-Thioxo-ester Rearrangements

Acylation of 4-aryl-3-mercapto-3-isothiazoline-5-thiones (1) with acid chloride in pyridine or alternatively with acid anhydride leads exclusively to 3-acylthio-4-aryl-3-isothiazoline-5-thiones (2).Reactions of (1) with reactive acetylenes afford 2-aryl(

THIOL-ESTER-THIONO-ESTER REARRANGEMENTS INDUCED BY ALKYLATING REAGENTS, PERACIDS, OR N-HALOSUCCINIMIDE IN THE 3-ACYLTHIO-4-ARYL-3-ISOTHIAZOLINE-5-THIONE SYSTEM

Alkylations of 3-acylthio-4-aryl-3-isothiazoline-5-thiones with diazomethane, triethyloxonium tetrafluoroborate, or alkyl iodide afford 5-alkylthio-4-aryl-3-thioacyloxyisothiazoles, whereas the reactions of these isothiazolines with peracids or N-halosucc