73311-70-3

Basic information

• Product Name: 1-Phenyl-3-phenylsulfanyl-2-vinyl-hexan-1-one
• CAS NO: 73311-70-3
• Molecular Weight: 310.46
• Mol File: 73311-70-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-Phenyl-3-phenylsulfanyl-2-vinyl-hexan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Phenyl-3-phenylsulfanyl-2-vinyl-hexan-1-one(73311-70-3)
• EPA Substance Registry System: 1-Phenyl-3-phenylsulfanyl-2-vinyl-hexan-1-one(73311-70-3)

Safety Data

• Hazardous Substances Data: 73311-70-3(Hazardous Substances Data)

Upstream product

• 72653-47-5 α-chlorobutyl phenyl sulfide 
• 124306-11-2 (Z)-trimethyl((1-phenylbuta-1,3-dien-1-yl)oxy)silane 
• 73311-48-5 trimethyl[(1-phenylbuta-1,3-dien-1-yl)oxy]silane 
• 930-69-8 sodium thiophenolate 
• 1126-80-3 (n-butylthio)benzene 

Relevant articles and documents

Some uses of silicon compounds in organic synthesis

1.The amount of γ-phenylthioalkylation of silyl dienol ethers is increased when the triphenylsilyl ether is used in place of the trimethylsilyl ether.Phenylthiomethylation is the least γ-selective carbon electrophile of several tried so far. 2.The acid-catalysed reactions of a range of γ-silyl tertiary alcohols cleanly give rearrangement, in which the silyl group controls the outcome.The reactions are similar in several respects to the rearrangements of the corresponding pinacols, except that the silicon controlled reactions are usually cleaner and give higher yields.The reaction is particularly useful for setting up quaternary carbon atoms.