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(1r,2s)-2-Sulfanylcyclopentanol

Base Information Edit
  • Chemical Name:(1r,2s)-2-Sulfanylcyclopentanol
  • CAS No.:5457-57-8
  • Molecular Formula:C5H10OS
  • Molecular Weight:118.2
  • Hs Code.:
  • NSC Number:24632
  • DSSTox Substance ID:DTXSID20282129
  • Wikidata:Q82016319
  • Mol file:5457-57-8.mol
(1r,2s)-2-Sulfanylcyclopentanol

Synonyms:5457-57-8;(1r,2s)-2-sulfanylcyclopentanol;NSC24632;SCHEMBL4300924;DTXSID20282129;NSC-24632

Suppliers and Price of (1r,2s)-2-Sulfanylcyclopentanol
Supply Marketing:Edit
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 3 raw suppliers
Chemical Property of (1r,2s)-2-Sulfanylcyclopentanol Edit
Chemical Property:
  • Vapor Pressure:0.0712mmHg at 25°C 
  • Boiling Point:202.5°Cat760mmHg 
  • Flash Point:76.3°C 
  • Density:1.11g/cm3 
  • XLogP3:0.8
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:118.04523611
  • Heavy Atom Count:7
  • Complexity:65.1
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC(C(C1)S)O
  • Isomeric SMILES:C1C[C@H]([C@H](C1)S)O
Technology Process of (1r,2s)-2-Sulfanylcyclopentanol

There total 6 articles about (1r,2s)-2-Sulfanylcyclopentanol 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:
Guidance literature:
With hydrazine hydrate; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1021/ja510069w
Guidance literature:
Multistep reaction; (i) AcSH, (ii) acid;
DOI:10.1021/ja00788a016
Refernces Edit
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