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1,2-Cyclopentanedicarboxylic acid, monomethyl ester, (1S,2S)-

Base Information Edit
  • Chemical Name:1,2-Cyclopentanedicarboxylic acid, monomethyl ester, (1S,2S)-
  • CAS No.:111138-48-8
  • Molecular Formula:C8H12O4
  • Molecular Weight:172.181
  • Hs Code.:
  • Mol file:111138-48-8.mol
1,2-Cyclopentanedicarboxylic acid, monomethyl ester, (1S,2S)-

Synonyms:(1S,2S)-Cyclopentane-1,2-dicarboxylic acid monomethyl ester;(1S,2S)-2-(methoxycarbonyl)cyclopentanecarboxylic acid;Rac-trans-cyclopentane-1,2-dicarboxylic acid monomethyl ester;trans-cyclopentane-1,2-dicarboxylic acid monomethyl ester;

Suppliers and Price of 1,2-Cyclopentanedicarboxylic acid, monomethyl ester, (1S,2S)-
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 1 raw suppliers
Chemical Property of 1,2-Cyclopentanedicarboxylic acid, monomethyl ester, (1S,2S)- Edit
Chemical Property:
  • PSA:63.60000 
  • LogP:0.66030 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 1,2-Cyclopentanedicarboxylic acid, monomethyl ester, (1S,2S)-

There total 5 articles about 1,2-Cyclopentanedicarboxylic acid, monomethyl ester, (1S,2S)- 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 4 steps
1.1: bromine / chloroform / 0 - 20 °C
1.2: 6 h / 0 °C
1.3: pH 5
2.1: acetic anhydride / 20 h / Reflux
3.1: 24 h / 60 °C / Inert atmosphere
4.1: lithium diisopropyl amide / 4 h / -78 °C / Inert atmosphere
With bromine; acetic anhydride; lithium diisopropyl amide; In chloroform;
Guidance literature:
Multi-step reaction with 3 steps
1: acetic anhydride / 20 h / Reflux
2: 24 h / 60 °C / Inert atmosphere
3: lithium diisopropyl amide / 4 h / -78 °C / Inert atmosphere
With acetic anhydride; lithium diisopropyl amide;
Refernces Edit
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