16660-57-4

Basic information

• Product Name: Cyclohexane, 1,1'-thiobis[2-chloro-
• CAS NO: 16660-57-4
• Molecular Formula: C12H20Cl2S
• Molecular Weight: 267.263
• Mol File: 16660-57-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Cyclohexane, 1,1'-thiobis[2-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexane, 1,1'-thiobis[2-chloro-(16660-57-4)
• EPA Substance Registry System: Cyclohexane, 1,1'-thiobis[2-chloro-(16660-57-4)

Safety Data

• Hazardous Substances Data: 16660-57-4(Hazardous Substances Data)

Upstream product

• 930-66-5 1-chlorocyclohexene 
• 7783-06-4 hydrogen sulfide 
• 75-18-3 dimethylsulfide 
• 110-83-8 cyclohexene 
• 6852-58-0 N-benzylidene tert-butylamine 
• 622-29-7 N-Benzylidenemethylamine 
• 538-51-2 benzylidene phenylamine 
• 28867-76-7 benzaldehyde benzylidenehydrazone 

Downstream Products

• 75917-86-1 bis(2-hydroxycyclohexyl)sulphide 
• 7133-46-2 dicyclohexyl sulfide 
• 75937-68-7 2-isobutyldicyclohexyl sulfide 
• 75937-69-8 bis(2-isobutylcyclohexyl) sulfide 
• 75937-71-2 bis(2-ethylcyclohexyl)sulfide 
• 2242-69-5 bis-(2-chloro-cyclohexyl)-sulfone 
• 34453-13-9 C₁₂H₂₀Cl₂OS 

Relevant articles and documents

Induced alkene reactions with sulfur dichloride. System sulfur dichloride - Dimethyl sulfide as a reagent for polysulfonation and conjugate chlorination of alkenes

In reaction of unsaturated compounds with sulfur dichloride in the presence of dimethyl sulfide radically new induced directions are realized: the reagent is involved as dimer or trimer (formation of di- and trisulfides). Alongside this process a conjugate chlorination occurred with participation of external nucleophiles, dimethyl sulfide and acetonitrile, furnishing sulfonium chlorides and N-substituted acetamides respectively. The relative importance of these alternative reactions depends on solvent, alkene structure, and order of reagents addition.