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1,3-Cyclohexanedicarboxylic acid, monoethyl ester, (1S,3R)-

Base Information Edit
  • Chemical Name:1,3-Cyclohexanedicarboxylic acid, monoethyl ester, (1S,3R)-
  • CAS No.:227783-03-1
  • Molecular Formula:C10H16O4
  • Molecular Weight:200.235
  • Hs Code.:
  • Mol file:227783-03-1.mol
1,3-Cyclohexanedicarboxylic acid, monoethyl ester, (1S,3R)-

Synonyms:1,3-Cyclohexanedicarboxylic acid,monoethyl ester,(1S,3R);

Suppliers and Price of 1,3-Cyclohexanedicarboxylic acid, monoethyl ester, (1S,3R)-
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
Total 5 raw suppliers
Chemical Property of 1,3-Cyclohexanedicarboxylic acid, monoethyl ester, (1S,3R)- Edit
Chemical Property:
  • PSA:66.43000 
  • LogP:0.10580 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 1,3-Cyclohexanedicarboxylic acid, monoethyl ester, (1S,3R)-

There total 1 articles about 1,3-Cyclohexanedicarboxylic acid, monoethyl ester, (1S,3R)- 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 pH 7 buffer; Pseudomonas cepacia PS-30 lipase; In water;
DOI:10.1016/S0957-4166(99)00060-9
Guidance literature:
Multi-step reaction with 2 steps
1: diphenylphosphoryl azide; triethylamine / toluene / 95 °C
2: aq. NaOH / tetrahydrofuran / 50 °C
With sodium hydroxide; diphenylphosphoranyl azide; triethylamine; In tetrahydrofuran; toluene; 1: Curtius rearrangement;
DOI:10.1016/j.bmc.2005.01.033
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