76216-50-7

Basic information

• Product Name: 1-(1-butylthio)-3-phenylpropane
• Synonyms: 1-(1-butylthio)-3-phenylpropane
• CAS NO: 76216-50-7
• Molecular Weight: 208.368
• Mol File: 76216-50-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(1-butylthio)-3-phenylpropane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-butylthio)-3-phenylpropane(76216-50-7)
• EPA Substance Registry System: 1-(1-butylthio)-3-phenylpropane(76216-50-7)

Safety Data

• Hazardous Substances Data: 76216-50-7(Hazardous Substances Data)

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 109-79-5 n-butanethiol 
• 629-45-8 dibutyl disulfide 
• 30076-98-3 (3,3-dimethoxypropyl)benzene 
• 103-25-3 3-phenylpropanoic acid methyl ester 
• 726-26-1 phenyl 3-phenylpropanoate 
• 501-52-0 3-Phenylpropionic acid 
• 300-57-2 allylbenzene 

Relevant articles and documents

Zinc-catalyzed regioselective addition of alkyl thiols to alkenes via anion or radical reactions

Zn-catalyzed reactions of alkenes with alkyl thiols could afford alkyl sulfides regioselectively. When the ZnI2- catalyzed hydrothiolation of alkenes was achieved using alkyl thiols at 100 °C, Markovnikov-type alkyl sulfides were obtained in excellent yields without the formation of linear products. To the contrary, Zn(OAc)2- catalyzed reaction gave rise only to anti-Markovnikov-type products regioselectively. The reaction proceeded via a radical process.

A novel approach to the practical synthesis of sulfides: An InBr 3-Et3SiH catalytic system promoted the direct reductive sulfidation of acetais with disulfides

We have demonstrated a facile and direct synthesis of sulfide derivatives using acetais and ketals, derived, from aromatic/ conjugated, aldehydes and aromatic ketones, with disulfides and the InBr3-Et3SiH reducing system., We also succeeded in developing an unprecedented one-pot preparation of an aliphatic sulfide from a disulfide and an aliphatic acetal. (Wiley-VCH Verlag GmbH & Co. KGaA.