41578-06-7

Basic information

• Product Name: Cyclohexane, 1-chloro-2-(methylthio)-, trans-
• CAS NO: 41578-06-7
• Molecular Formula: C7H13ClS
• Molecular Weight: 164.699
• Mol File: 41578-06-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Cyclohexane, 1-chloro-2-(methylthio)-, trans-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexane, 1-chloro-2-(methylthio)-, trans-(41578-06-7)
• EPA Substance Registry System: Cyclohexane, 1-chloro-2-(methylthio)-, trans-(41578-06-7)

Safety Data

• Hazardous Substances Data: 41578-06-7(Hazardous Substances Data)

Upstream product

• 67-68-5 dimethyl sulfoxide 
• 110-83-8 cyclohexene 
• 2425-33-4 2-bromocyclocyclohexanol 
• 41578-04-5 1-hydroxy-2-methylthiocyclohexane 
• 5813-48-9 Methanesulfenyl chloride 

Downstream Products

• 41578-02-3 trans-1-Methoxy-2-methylthiocyclohexane 
• 130925-42-7 trans-1-Fluoro-2-methylsulfonylcyclohexane 
• 59059-66-4 trans-1-(methylsulfonyl)-2-bromocyclohexane 
• 41578-03-4 trans-1-methoxy-2-(methylsulfonyl)cyclohexane 
• 130925-39-2 trans-1-Fluoro-2-methylsulfinylcyclohexane 
• 130925-39-2 trans-1-Fluoro-2-methylsulfinylcyclohexane 
• 130925-41-6 trans-1-Broro-2-methylsulfinylcyclohexane 
• 130925-41-6 trans-1-Broro-2-methylsulfinylcyclohexane 
• 41578-04-5 1-hydroxy-2-methylthiocyclohexane 
• 130925-36-9 trans-1-Iodo-2-methylthiocyclohexane 
• 122895-30-1 trans-1-Fluoro-2-(methylthio)cyclohexane 
• 41578-07-8 trans-1-Methylthio-2-bromocyclohexane 
• 34046-61-2 3-Methylthio-1-cyclohexene 

Relevant articles and documents

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Metal-Free Chlorothiolation of Alkenes Using HCl and Sulfoxides

We report a novel method for the chlorothiolation of alkenes using HCl and sulfoxides to achieve the 1,2-difunctionalization of unactivated alkenes. The combination of our new HCl reagent (HCl/DMPU) with sulfoxides forms a unique chlorothiolation system.

Conformational analysis of 1-Y, 2-Z-cyclohexanes ( Y = OH, OMe, F, Cl, Br and I; Z= SMe, SOMe and SO2Me): Study of the Z/Y gauche interactions

The conformational study of the title compounds is reported. The configurational assignment of the epimeric sulfoxides was based on the relationship between the stereochemistry of the sulfinyl group and the chemical shifts of the neighboring nuclei. The v