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5-Tetradecenoic acid, methyl ester, (Z)-

Base Information Edit
  • Chemical Name:5-Tetradecenoic acid, methyl ester, (Z)-
  • CAS No.:28369-26-8
  • Molecular Formula:C15H28O2
  • Molecular Weight:240.386
  • Hs Code.:
  • Mol file:28369-26-8.mol
5-Tetradecenoic acid, methyl ester, (Z)-

Synonyms:cis-5-Tetradecensaeuremethylester;methyl(Z)-5-tetra-decanoate;

Suppliers and Price of 5-Tetradecenoic acid, methyl ester, (Z)-
Supply Marketing:Edit
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
  • TRC
  • cis-5-TetradecenoicAcidMethylEster
  • 25mg
  • $ 165.00
  • Medical Isotopes, Inc.
  • cis-5-TetradecenoicAcidMethylEster
  • 250 mg
  • $ 2200.00
Total 0 raw suppliers
Chemical Property of 5-Tetradecenoic acid, methyl ester, (Z)- Edit
Chemical Property:
  • PSA:26.30000 
  • LogP:4.63650 
Purity/Quality:

cis-5-TetradecenoicAcidMethylEster *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses cis-5-Tetradecenoic Acid Methyl Ester is an intermediate in the synthesis of long-chain saturated fatty acids.
Technology Process of 5-Tetradecenoic acid, methyl ester, (Z)-

There total 10 articles about 5-Tetradecenoic acid, methyl ester, (Z)- 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:
Multi-step reaction with 3 steps
1: 86 percent / dimethylsulfoxide / Ambient temperature
2: KOH / ethane-1,2-diol / 6 h / Heating
With potassium hydroxide; In ethylene glycol; dimethyl sulfoxide;
Guidance literature:
Multi-step reaction with 2 steps
1: KOH / ethane-1,2-diol / 6 h / Heating
With potassium hydroxide; In ethylene glycol;
Guidance literature:
Multi-step reaction with 5 steps
1: triethylamine / CH2Cl2 / 1) 0 deg C, 0.5 h, 2) RT, 6 h
2: LiBr / acetone / 5 h / Ambient temperature
3: 86 percent / dimethylsulfoxide / Ambient temperature
4: KOH / ethane-1,2-diol / 6 h / Heating
With potassium hydroxide; triethylamine; lithium bromide; In dichloromethane; ethylene glycol; dimethyl sulfoxide; acetone;
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