(1R,2R)-1-Chloro-2-(ethylsulfanyl)cyclohexane

Base Information

Chemical Name:(1R,2R)-1-Chloro-2-(ethylsulfanyl)cyclohexane
CAS No.:20556-30-3
Molecular Formula:C8H15ClS
Molecular Weight:178.726
Hs Code.:
DSSTox Substance ID:DTXSID30531519
Wikidata:Q82403444

Synonyms:20556-30-3;(1R,2R)-1-Chloro-2-(ethylsulfanyl)cyclohexane;DTXSID30531519

Suppliers and Price of (1R,2R)-1-Chloro-2-(ethylsulfanyl)cyclohexane

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
Packaging
price

Total 0 raw suppliers

Chemical Property of (1R,2R)-1-Chloro-2-(ethylsulfanyl)cyclohexane

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:178.0582993
Heavy Atom Count:10
Complexity:95.3

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCSC1CCCCC1Cl
Isomeric SMILES:CCS[C@@H]1CCCC[C@H]1Cl

Technology Process of (1R,2R)-1-Chloro-2-(ethylsulfanyl)cyclohexane

There total 3 articles about (1R,2R)-1-Chloro-2-(ethylsulfanyl)cyclohexane 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: 62.0%

: 58198-41-7,613258-12-1
trans-2-ethylsulfanyl-cyclohexanol

: 20556-30-3
trans-2-chloro-1-ethylthiocyclohexane

Guidance literature:: With triphenylphosphine; In tetrachloromethane; at 77 ℃;
DOI:10.1021/jo00141a036

Reference yield:

: 286-20-4
cyclohexane-1,2-epoxide

: 20556-30-3
trans-2-chloro-1-ethylthiocyclohexane

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / NaOC₂H₅ / ethanol / 18 h / Heating

2: 62 percent / triphenylphosphine / CCl₄ / 77 °C

With sodium ethanolate; triphenylphosphine; In tetrachloromethane; ethanol;
DOI:10.1021/jo00141a036