1191415-24-3

Basic information

• Product Name: 2-(2,2-dibromovinyl)benzenethiol
• Synonyms: 2-(2,2-dibromovinyl)benzenethiol
• CAS NO: 1191415-24-3
• Molecular Weight: 294.01
• Mol File: 1191415-24-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(2,2-dibromovinyl)benzenethiol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,2-dibromovinyl)benzenethiol(1191415-24-3)
• EPA Substance Registry System: 2-(2,2-dibromovinyl)benzenethiol(1191415-24-3)

Safety Data

• Hazardous Substances Data: 1191415-24-3(Hazardous Substances Data)

Upstream product

• 1191415-55-0 (1-tert-butylsulfanyl)-2-(2,2-dibromovinyl)benzenethiol 
• 89-98-5 2-chloro-benzaldehyde 
• 65924-65-4 2-(tert-butylthio)benzaldehyde 

Downstream Products

• 1196-81-2 2-ethylbenzo[b]thiophene 
• 28684-74-4 2-[(E)-2-phenylvinyl]-1-benzothiophene 
• 936734-96-2 2-(4-fluoro-phenyl)-benzo[b]thiophene 
• 55084-51-0 2-(2-methylphenyl)-1-benzothiophene 
• 1192716-41-8 2-(3-chlorophenyl)-1-benzothiophene 
• 1207-95-0 2-phenylbenzo[b]thiophene 
• 161886-97-1 2-(3-nitrophenyl)-1-benzothiophene 
• 133617-45-5 2-(3',4'-dimethoxyphenyl)benzothiophene 
• 132932-62-8 2-(p-acetylphenyl)benzothiophene 
• 106276-69-1 2-(phenylthio)benzo[b]thiophene 
• 866849-52-7 phenyl benzo[b]thiophene-2-carboxylate 
• 17890-55-0 ethyl benzo[b]thiophene-2-carboxylate 
• 5394-13-8 2-bromo-1-benzothiophene 
• 22913-24-2 methyl benzo[b]thiophene-2-carboxylate 

Relevant articles and documents

Palladium-Catalyzed Domino Cyclization/Phosphorylation of gem-Dibromoolefins with P(O)H Compounds: Synthesis of Phosphorylated Heteroaromatics

We presented a palladium-catalyzed domino cyclization/phosphorylation of gem-dibromoolefins, which utilize H-phosphinates and secondary phosphine oxides as the phosphine sources, respectively. A variety of phosphorylated heteroaromatics were obtained in m

Intramolecular cross-coupling of gem-dibromoolefins: A mild approach to 2-bromo benzofused heterocycles

Highly useful halogenated benzofurans and benzothiophenes are prepared from readily available gem-dibromoolefins using a mild, ligand-free copper catalyzed cross-coupling procedure.