tert-Butyl cyclohexyl sulfide

Base Information

Chemical Name:tert-Butyl cyclohexyl sulfide
CAS No.:7133-23-5
Molecular Formula:C10H20S
Molecular Weight:172.3308
Hs Code.:2930909090
Mol file:7133-23-5.mol

Synonyms:Sulfide,tert-butyl cyclohexyl;tert-Butyl-cyclohexyl-sulfid;(tert-Butylsulfanyl)cyclohexane;tert-Butyl cyclohexyl sulfide;

Suppliers and Price of tert-Butyl cyclohexyl sulfide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 5 raw suppliers

Chemical Property of tert-Butyl cyclohexyl sulfide

Chemical Property:

Vapor Pressure:0.0903mmHg at 25°C
Boiling Point:232.3°Cat760mmHg
Flash Point:83.9°C
PSA：25.30000
Density:0.9g/cm³
LogP:3.85080

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of tert-Butyl cyclohexyl sulfide

There total 3 articles about tert-Butyl cyclohexyl sulfide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

: 1569-69-3
Cyclohexanethiol

: 691-64-5
di-tert-butyl oxalate

: 7133-23-5
tert-butyl(cyclohexyl)sulfane

Guidance literature:: With copper(II) bis(trifluoromethanesulfonate); In 1,2-dichloro-ethane; at 40 ℃; for 12h; Solvent; Reagent/catalyst; Catalytic behavior; Sealed tube; Schlenk technique;
DOI:10.1021/acs.orglett.0c04206

Reference yield:

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

: 75-66-1
2-methylpropan-2-thiol

: 7133-23-5
tert-butyl(cyclohexyl)sulfane

Guidance literature:: With triethylsilane; boron trifluoride; Yield given. Multistep reaction; 1.) CH₂Cl₂, 0 deg C, 1 min, 2.) 0 deg C to r.t., 3 h;
DOI:10.1055/s-1992-26138