39984-84-4

Basic information

• Product Name: Benzene, (5-hexenylthio)-
• CAS NO: 39984-84-4
• Molecular Formula: C12H16S
• Molecular Weight: 192.325
• Mol File: 39984-84-4.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: Benzene, (5-hexenylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (5-hexenylthio)-(39984-84-4)
• EPA Substance Registry System: Benzene, (5-hexenylthio)-(39984-84-4)

Safety Data

• Hazardous Substances Data: 39984-84-4(Hazardous Substances Data)

Upstream product

• 1212-08-4 S-Phenyl benzenethiosulfonate 
• 2695-47-8 6-Bromo-1-hexene 
• 4551-15-9 phenylthiotrimethylsilane 
• 71138-63-1 (5-hexenyloxy)trimethylsilane 
• 5048-26-0 5-hexenyl acetate 
• 821-41-0 5-Hexen-1-ol 
• 34884-33-8 (phenylthio)-methylenetriphenylphosphorane 
• 2100-17-6 4-pentenal 
• 108-98-5 thiophenol 
• 125115-14-2 1-chloro-1-phenylsulfanyl-5-hexene 
• 3561-67-9 bis(phenylthio)methane 
• 7766-48-5 1-iodo-4-pentene 
• 930-69-8 sodium thiophenolate 
• 63668-13-3 Δ⁵-hexenylmercury chloride 

Downstream Products

• 110117-63-0 trans-3-(phenylsylfonyl)cyclohexanol acetate 
• 110117-63-0 cis-3-(phenylsulfonyl)cyclohexanol acetate 
• 65288-09-7 3-Benzenesulfonyl-cyclohexanol 
• 110117-57-2 (2-Benzenesulfonyl-cyclopentyl)-methanol 
• 125115-16-4 6,6-bis(phenylthio)-1-hexene 
• 110434-51-0 trans-1-methyl-2-(phenylthio)cyclopentane 
• 110434-51-0 cis-1-methyl-2-(phenylthio)cyclopentane 
• 106201-03-0 cis-1-benzenesulfonyl-2-methyl cyclopentane 
• 106201-03-0 1-benzenesulfonyl-2-methylcyclopentane 
• 132398-39-1 cis-2-methylcyclopentyl phenyl sulfoxide 
• 132398-39-1 trans-2-methylcyclopentyl phenyl sulfoxide 
• 132398-38-0 6-chloro-6-phenylsulfonyl-1-hexene 
• 193097-39-1 6-chloro-6-phenylsulfinyl-1-hexene 
• 132398-40-4 1-(hex-5-enylsulfinyl)benzene 

Relevant articles and documents

Electroreductive Nickel-Catalyzed Thiolation: Efficient Cross-Electrophile Coupling for C?S Formation

Sulfur-containing molecules are of utmost topical importance towards the effective development of pharmaceuticals and functional materials. Herein, we present an efficient and mild electrochemical thiolation by cross-electrophile coupling of alkyl bromide

Synthesis of thioethers by ini3-catalyzed substitution of siloxy group using thiosilanes

The substitution of a siloxy group using thiosilanes smoothly occurred in the presence of InI3 catalyst to yield the corresponding thioethers. InI3was a specifically effective catalyst in this reaction system, while other typical Lew

Synthesis of a wide range of thioethers by indium triiodide catalyzed direct coupling between alkyl acetates and thiosilanes

An indium triiodide-catalyzed substitution of the acetoxy group in alkyl acetates with thiosilanes provides access to a variety of thioethers. The method is efficient for a wide scope of acetates such as primary alkyl, secondary alkyl, tertiary alkyl, allylic, benzylic, and propargylic acetates.