114744-69-3

Basic information

• Product Name: S-(2-phenyl carbamoyl benzeneselenenyl)benzylmercaptan
• Synonyms: S-(2-phenyl carbamoyl benzeneselenenyl)benzylmercaptan
• CAS NO: 114744-69-3
• Molecular Weight: 398.387
• Mol File: 114744-69-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: S-(2-phenyl carbamoyl benzeneselenenyl)benzylmercaptan(CAS DataBase Reference)
• NIST Chemistry Reference: S-(2-phenyl carbamoyl benzeneselenenyl)benzylmercaptan(114744-69-3)
• EPA Substance Registry System: S-(2-phenyl carbamoyl benzeneselenenyl)benzylmercaptan(114744-69-3)

Safety Data

• Hazardous Substances Data: 114744-69-3(Hazardous Substances Data)

Upstream product

• 104473-83-8 2-phenyl-1,2-benzioselenazol-3(2H)-one selenoxide 
• 100-53-8 phenylmethanethiol 
• 542-92-7 cyclopenta-1,3-diene 
• 60940-34-3 2-phenyl-1,2-benzoisoselenazol-3(2H)-one 

Downstream Products

• 60940-34-3 2-phenyl-1,2-benzoisoselenazol-3(2H)-one 
• 101562-89-4 S-(2-phenyl carbamoyl benzeneselenenyl)-glutathione 
• 104030-64-0 C₁₅H₁₅NOSSe 
• 106663-84-7 2,2‘-diselenobis(N-phenylbenzamide) 

Relevant articles and documents

Nucleophilic cleavage of selenaheterocyclic ring in benzisoselenazol-3(2H)- ones and 1,3,2-benzodiselenazoles

The reactions of cyclic selenenamides: benzisoselenazol-3(2H)-ones and 1,3,2-benzo-diselenazoles 3 with living cell nucleophiles such as water and thiols were investigated. Both of them caused Se-N bond cleavage. The thiolysis of 1 led to selenosulphides

MECHANISM OF THE CATALYTIC REDUCTION OF HYDROPEROXIDES BY EBSELEN : A SELENIUM - 77 NMR STUDY

Ebselen (2-phenyl-1,2-benzisoselenazol-3(2H)-one 1, a non-toxic selenium containing heterocyclic compound has been shown to display both anti-inflammatory activity in vivo and GSH-Px-like activity in vitro.Using (1)H and (77)Se NMr we investigated the mechanism of reduction of hydroperoxides by thiols in the presence of 1.A catalytic cycle depending on the formation of diselenides and selenylsulfides was found.The selenic acid oxidation level present in compound 1 is particularly stable because of the intermolecular cyclisation.This contracts with previously reported results concerning the oxidation of organoselenium compounds.