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Hexadec-7-enol

Base Information Edit
  • Chemical Name:Hexadec-7-enol
  • CAS No.:24546-19-8
  • Molecular Formula:C16H32O
  • Molecular Weight:240.429
  • Hs Code.:
  • DSSTox Substance ID:DTXSID701316792
  • Wikidata:Q110077191
  • Mol file:24546-19-8.mol
Hexadec-7-enol

Synonyms:hexadec-7-enol;DTXSID701316792;AKOS030255027;24546-19-8

Suppliers and Price of Hexadec-7-enol
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Hexadec-7-enol Edit
Chemical Property:
  • XLogP3:6.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:13
  • Exact Mass:240.245315640
  • Heavy Atom Count:17
  • Complexity:152
Purity/Quality:
Safty Information:
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MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCC=CCCCCCCO
Technology Process of Hexadec-7-enol

There total 35 articles about Hexadec-7-enol 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 quinoline; hydrogen; In cyclohexane; at 20 ℃; for 2h; under 760.051 Torr; stereoselective reaction;
DOI:10.1016/j.tet.2012.03.002
Guidance literature:
hexadec-7-yn-1-ol; With lithium aluminium tetrahydride; In tetrahydrofuran; diethylene glycol dimethyl ether; at 10 - 140 ℃; Inert atmosphere;
With water; In tetrahydrofuran; diethylene glycol dimethyl ether; stereoselective reaction; Cooling with ice;
DOI:10.1016/j.tet.2012.03.002
Guidance literature:
With sodium methylsulfinylmethanide; In tetrahydrofuran; dimethyl sulfoxide; at 5 ℃; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1080/00021369.1980.10864303
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