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Glycidyl oleate, (S)-

Base Information
  • Chemical Name:Glycidyl oleate, (S)-
  • CAS No.:849589-85-1
  • Molecular Formula:C21H38O3
  • Molecular Weight:338.531
  • Hs Code.:
  • UNII:JB5GHF083M
  • Nikkaji Number:J2.148.586A
Glycidyl oleate, (S)-

Synonyms:Glycidyl oleate, (S)-;Glycidyl oleate, (+)-;JB5GHF083M;UNII-JB5GHF083M;849589-85-1;9-Octadecenoic acid (9Z)-, (2S)-2-oxiranylmethyl ester;Oleoyl[(S)-glycidyl] ether

Suppliers and Price of Glycidyl oleate, (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 Glycidyl oleate, (S)-
Chemical Property:
  • XLogP3:7.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:18
  • Exact Mass:338.28209507
  • Heavy Atom Count:24
  • Complexity:325
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCCCCCCCC=CCCCCCCCC(=O)OCC1CO1
  • Isomeric SMILES:CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H]1CO1
Technology Process of Glycidyl oleate, (S)-

There total 1 articles about Glycidyl oleate, (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:
With dmap; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; at 20 ℃;
DOI:10.1016/j.tetlet.2006.08.066
Guidance literature:
Multi-step reaction with 2 steps
1: 97 percent / trifluoroacetic anhydride / tetrahydrofuran; CH2Cl2 / 5 h / 80 °C
2: 0.338 g / pyridine; methanol / CH2Cl2; pentane / 0.33 h / 0 - 20 °C
With pyridine; methanol; trifluoroacetic anhydride; In tetrahydrofuran; dichloromethane; pentane;
DOI:10.1016/j.tetlet.2005.01.093
Guidance literature:
Multi-step reaction with 2 steps
1: 91 percent / trimethylsilyl chloride / 5 h / 20 °C
2: 0.374 g / pyridine; methanol / pentane; CH2Cl2 / 0.33 h / 20 °C
With pyridine; methanol; chloro-trimethyl-silane; In dichloromethane; pentane;
DOI:10.1055/s-2006-948206
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