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(S)-1-Cyclohexylpropan-1-amine

Base Information
  • Chemical Name:(S)-1-Cyclohexylpropan-1-amine
  • CAS No.:19146-53-3
  • Molecular Formula:C9H19N
  • Molecular Weight:141.25386
  • Hs Code.:
  • DSSTox Substance ID:DTXSID701296160
  • Nikkaji Number:J58.453C
  • Mol file:19146-53-3.mol
(S)-1-Cyclohexylpropan-1-amine

Synonyms:(S)-1-Cyclohexylpropan-1-amine;19146-53-3;(1S)-1-cyclohexylpropan-1-amine;SCHEMBL5908926;DTXSID701296160;AKOS006368185;(alphaS)-alpha-Ethylcyclohexanemethanamine;N10674

Suppliers and Price of (S)-1-Cyclohexylpropan-1-amine
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 5 raw suppliers
Chemical Property of (S)-1-Cyclohexylpropan-1-amine
Chemical Property:
  • PSA:26.02000 
  • LogP:3.00430 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:141.151749610
  • Heavy Atom Count:10
  • Complexity:84.7
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCC(C1CCCCC1)N
  • Isomeric SMILES:CC[C@@H](C1CCCCC1)N
Technology Process of (S)-1-Cyclohexylpropan-1-amine

There total 9 articles about (S)-1-Cyclohexylpropan-1-amine 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 potassium hydroxide; hydrogen; palladium on activated charcoal; In methanol;
DOI:10.1016/j.tet.2005.08.064
Guidance literature:
Multi-step reaction with 3 steps
1: 92 percent / copper(I) bromide; (R)-Quinap; molecular sieves 4 Angstroem / toluene; decane / 20 °C
2: 93 percent / Bu4NF / tetrahydrofuran / 0 °C
3: 84 percent / KOH; H2 / Pd on charcoal / methanol
With (R)-1-(2-(diphenylphosphanyl)naphthalen-1-yl)isoquinoline; potassium hydroxide; 4 A molecular sieve; tetrabutyl ammonium fluoride; hydrogen; copper(I) bromide; palladium on activated charcoal; In tetrahydrofuran; methanol; decane; toluene;
DOI:10.1016/j.tet.2005.08.064
Guidance literature:
Multi-step reaction with 2 steps
1: 93 percent / Bu4NF / tetrahydrofuran / 0 °C
2: 84 percent / KOH; H2 / Pd on charcoal / methanol
With potassium hydroxide; tetrabutyl ammonium fluoride; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1016/j.tet.2005.08.064
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