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Cyclopentanecarboxylic acid, 1-(2-methyl-1-oxopropyl)-, methyl ester (9CI)

Base Information
  • Chemical Name:Cyclopentanecarboxylic acid, 1-(2-methyl-1-oxopropyl)-, methyl ester (9CI)
  • CAS No.:807336-32-9
  • Molecular Formula:C11H18O3
  • Molecular Weight:198.262
  • Hs Code.:
  • Mol file:807336-32-9.mol
Cyclopentanecarboxylic acid, 1-(2-methyl-1-oxopropyl)-, methyl ester (9CI)

Synonyms:Cyclopentanecarboxylic acid, 1-(2-methyl-1-oxopropyl)-, methyl ester (9CI)

Suppliers and Price of Cyclopentanecarboxylic acid, 1-(2-methyl-1-oxopropyl)-, methyl ester (9CI)
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Chemical Property of Cyclopentanecarboxylic acid, 1-(2-methyl-1-oxopropyl)-, methyl ester (9CI)
Chemical Property:
  • Boiling Point:107 - 109 °C (13 mmHg) 
  • PSA:43.37000 
  • LogP:1.94490 
Purity/Quality:
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MSDS Files:

SDS file from LookChem

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Technology Process of Cyclopentanecarboxylic acid, 1-(2-methyl-1-oxopropyl)-, methyl ester (9CI)

There total 1 articles about Cyclopentanecarboxylic acid, 1-(2-methyl-1-oxopropyl)-, methyl ester (9CI) 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 2 steps
1: 86 percent / bromine / acetic acid / 1.5 h / Heating
2: 58 percent / Zn; HgCl2 / ethyl acetate / 1 h / Heating
With bromine; mercury dichloride; zinc; In acetic acid; ethyl acetate; 2: Reformatsky reaction;
DOI:10.1023/B:RUJO.0000036083.25649.fa
Guidance literature:
Multi-step reaction with 2 steps
1: 86 percent / bromine / acetic acid / 1.5 h / Heating
2: 52 percent / Zn; HgCl2 / ethyl acetate / 1 h / Heating
With bromine; mercury dichloride; zinc; In acetic acid; ethyl acetate; 2: Reformatsky reaction;
DOI:10.1023/B:RUJO.0000036083.25649.fa
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