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Cyclohexanol, 1-(1-phenyl-2-propenyl)-

Base Information
  • Chemical Name:Cyclohexanol, 1-(1-phenyl-2-propenyl)-
  • CAS No.:79801-99-3
  • Molecular Formula:C15H20O
  • Molecular Weight:216.323
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90466151
  • Nikkaji Number:J979.003I
Cyclohexanol, 1-(1-phenyl-2-propenyl)-

Synonyms:Cyclohexanol, 1-(1-phenyl-2-propenyl)-;79801-99-3;DTXSID90466151;1-(1-phenyl-2-propenyl)cyclohexanol;AKOS015906492;1-(1-phenyl-prop-2-enyl)-cyclohexan-1-ol

Suppliers and Price of Cyclohexanol, 1-(1-phenyl-2-propenyl)-
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 1 raw suppliers
Chemical Property of Cyclohexanol, 1-(1-phenyl-2-propenyl)-
Chemical Property:
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:3
  • Exact Mass:216.151415257
  • Heavy Atom Count:16
  • Complexity:222
Purity/Quality:

85.0-99.8% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C=CC(C1=CC=CC=C1)C2(CCCCC2)O
Technology Process of Cyclohexanol, 1-(1-phenyl-2-propenyl)-

There total 21 articles about Cyclohexanol, 1-(1-phenyl-2-propenyl)- 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 Cp*2Sm(THF)2; In toluene; for 20h; Ambient temperature;
DOI:10.1021/jo9723016
Guidance literature:
With zinc; In N,N-dimethyl-formamide; for 0.5h; Ambient temperature;
Guidance literature:
In tetrahydrofuran; at 20 ℃; for 1h; regioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201207951
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