64741-03-3

Basic information

• Product Name: Benzene, [(2-chlorocyclopentyl)thio]-, trans-
• CAS NO: 64741-03-3
• Molecular Formula: C11H13ClS
• Molecular Weight: 212.743
• Mol File: 64741-03-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, [(2-chlorocyclopentyl)thio]-, trans-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(2-chlorocyclopentyl)thio]-, trans-(64741-03-3)
• EPA Substance Registry System: Benzene, [(2-chlorocyclopentyl)thio]-, trans-(64741-03-3)

Safety Data

• Hazardous Substances Data: 64741-03-3(Hazardous Substances Data)

Upstream product

• 930-29-0 1-chlorocyclopent-1-ene 
• 108-98-5 thiophenol 
• 142-29-0 cyclopentene 
• 931-59-9 benzenesulfenyl chloride 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 64740-90-5 1-cyclopenten-1-yl phenyl sulfone 
• 3467-68-3 3-(phenylthio)cyclopentene 
• 37053-16-0 cyclopent-1-en-1-yl (phenyl) sulfide 
• 5296-64-0 allyl phenyl thioether 
• 89113-67-7 ((1S,2R)-2-Allyl-cyclopentylsulfanyl)-benzene 
• 86769-72-4 ((1R,2S)-2-Phenylsulfanyl-cyclopentyl)-acetic acid methyl ester 
• 110434-51-0 trans-1-methyl-2-(phenylthio)cyclopentane 
• 86769-74-6 2-((1R,2S)-2-Phenylsulfanyl-cyclopentyl)-propionic acid ethyl ester 
• 86769-73-5 2-Methyl-2-((1S,2R)-2-phenylsulfanyl-cyclopentyl)-propionic acid methyl ester 
• 64741-14-6 (+/-)-trans-1-benzenesulfonyl-2-chloro-cyclopentane 
• 64741-14-6 (+/-)-cis-1-benzenesulfonyl-2-chloro-cyclopentane 

Relevant articles and documents

Regioselective Chlorothiolation of Alkenes with Sulfonyl Chlorides

Newly developed sulfonyl chloride-based regioselective chlorothiolation of alkenes has been disclosed; the reaction is compatible with a variety of functional groups and can be scaled up to the gram scale with no loss in yield. The employment of readily a

O-SILYLATED ENOLATES IN ORGANIC SYNTHESIS: SULPHUR-MEDIATED ALKYLATION OF ESTERS WITH ALKENES.

O-Silylated ester enolates can be alkylated, under ZnBr2-catalysis, by the PhSCl-adducts of mono- and di-substituted alkenes to give γ-phenylthioesters, from which sulphur can be removed both reductively and oxidatively.This alkene carbosulphenylation rea