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Cimepanol, (S)-

Base Information
  • Chemical Name:Cimepanol, (S)-
  • CAS No.:62039-13-8
  • Molecular Formula:C10H20O
  • Molecular Weight:156.268
  • Hs Code.:
  • UNII:M40ON86QX2
  • Nikkaji Number:J58.851B
Cimepanol, (S)-

Synonyms:Cimepanol, (S)-;M40ON86QX2;UNII-M40ON86QX2;62039-13-8;Cyclohexanemethanol, alpha-(1-methylethyl)-, (alphaS)-;SCHEMBL10304687;(S)-1-Cyclohexyl-2-methylpropane-1-ol;CYCLOHEXANEMETHANOL, .ALPHA.-(1-METHYLETHYL)-, (.ALPHA.S)-

Suppliers and Price of Cimepanol, (S)-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of Cimepanol, (S)-
Chemical Property:
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:156.151415257
  • Heavy Atom Count:11
  • Complexity:103
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C)C(C1CCCCC1)O
  • Isomeric SMILES:CC(C)[C@@H](C1CCCCC1)O
Technology Process of Cimepanol, (S)-

There total 6 articles about Cimepanol, (S)- 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:
isopropylmagnesium chloride; With sodium methylate; zinc(II) chloride; In diethyl ether; at 0 - 20 ℃; Inert atmosphere;
cyclohexanecarbaldehyde; With (S)-N-(3-methyl-1-(1-pyrrolidin-1-yl)butan-2-yl) diphenylphosphinic amideamine; at 20 ℃; optical yield given as %ee; enantioselective reaction; Inert atmosphere; Neat (no solvent);
DOI:10.1039/c0cc01301c
Guidance literature:
With C17H38BFeNOP2; hydrogen; In ethanol; at 60 ℃; for 6h; under 22502.3 Torr; Reagent/catalyst; Solvent; Temperature; Overall yield = 51 %; Optical yield = 32 %ee; enantioselective reaction; Autoclave;
DOI:10.1002/adsc.201801511
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