91789-07-0

Basic information

• Product Name: Benzene, (2-octenylthio)-, (Z)-
• CAS NO: 91789-07-0
• Molecular Formula: C14H20S
• Molecular Weight: 220.379
• Mol File: 91789-07-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzene, (2-octenylthio)-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (2-octenylthio)-, (Z)-(91789-07-0)
• EPA Substance Registry System: Benzene, (2-octenylthio)-, (Z)-(91789-07-0)

Safety Data

• Hazardous Substances Data: 91789-07-0(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 5296-64-0 allyl phenyl thioether 
• 20739-58-6 2-octyn-1-ol 
• 628-71-7 1-Heptyne 
• 628-17-1 amyl iodide 
• 110-53-2 1-Bromopentane 
• 3391-86-4 1-octen-3-ol 
• 26001-58-1 (Z)-oct-2-en-1-ol 
• 14204-24-1 N-(phenylthio)succinimide 
• 36602-98-9 2-(oct-2-yn-1-yloxy)tetrahydro-2H-pyran 
• 79243-01-9 3-(phenylthio)oct-1-ene 
• 25466-54-0 (Z)-1-bromo-2-octene 
• 4551-15-9 phenylthiotrimethylsilane 

Downstream Products

• 113460-93-8 (1'R*,2'E,3R*)-3-<1'-(phenylsulfonyl)oct-2'-enyl>butan-4-olide 
• 113460-93-8 (1'R*,2'Z,3R*)-3-<1'-(phenylsulfonyl)oct-2'-enyl>butan-4-olide 
• 113460-93-8 (1'S*,2'E,3R*)-3-<1'-(phenylsulfonyl)oct-2'-enyl>butan-4-olide 
• 113460-93-8 (1'S*,2'Z,3R*)-3-<1'-(phenylsulfonyl)oct-2'-enyl>butan-4-olide 
• 113460-94-9 (1'S*,2'E,3R*)-3-<3'-(phenylsulfonyl)-1'-pentylprop-2'-enyl>butan-4-olide 
• 113460-94-9 (1'R*,2'E,3R*)-3-<3'-(phenylsulfonyl)-1'-pentylprop-2'-enyl>butan-4-olide 
• 91940-09-9 (E)-(oct-2-en-1-ylsulfonyl)benzene 
• 86823-71-4 (Z)-1-(phenylsulfonyl)oct-2-ene 

Relevant articles and documents

Direct synthesis of allyl sulfides from allyl alcohols and thiols

In the presence of boron trifluoride-diethyl ether complex, various allyl alcohols [(-)-myrtenol, geraniol, cinnamyl alcohol, linalool, 1-octen-3-ol, 2-hydroxybenzyl alcohol and bicyclic diols] were reacted with thiophenol, 1-butanethiol, trimethyl(phenylthio)silane or hexamethylsilane in dichloromethane at room temperature to give the corresponding allyl sulfides in good to excellent yields. The mild conditions for this transformation allowed chemoselectivity.