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Cyclopentanecarboxylic acid, 1-(1-methylethyl)-3-oxo-, (1S)- (9CI)

Base Information
  • Chemical Name:Cyclopentanecarboxylic acid, 1-(1-methylethyl)-3-oxo-, (1S)- (9CI)
  • CAS No.:782493-13-4
  • Molecular Formula:C9H14 O3
  • Molecular Weight:170.20566
  • Hs Code.:2918300090
  • Mol file:782493-13-4.mol
Cyclopentanecarboxylic acid, 1-(1-methylethyl)-3-oxo-, (1S)- (9CI)

Synonyms:Cyclopentanecarboxylic acid, 1-(1-methylethyl)-3-oxo-, (1S)- (9CI)

Suppliers and Price of Cyclopentanecarboxylic acid, 1-(1-methylethyl)-3-oxo-, (1S)- (9CI)
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Total 2 raw suppliers
Chemical Property of Cyclopentanecarboxylic acid, 1-(1-methylethyl)-3-oxo-, (1S)- (9CI)
Chemical Property:
  • PSA:54.37000 
  • LogP:1.46640 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of Cyclopentanecarboxylic acid, 1-(1-methylethyl)-3-oxo-, (1S)- (9CI)

There total 23 articles about Cyclopentanecarboxylic acid, 1-(1-methylethyl)-3-oxo-, (1S)- (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:
With palladium on carbon; hydrogen; In methanol; under 760.051 Torr;
DOI:10.1021/ml900009d
Guidance literature:
aminoacid salt; With N-Bromosuccinimide; sodium hydrogencarbonate; In dichloromethane; at 0 ℃; for 4h;
With ethanol; sodium methylate; for 1h; Heating / reflux;
With sulfuric acid; water; at 0 - 20 ℃; for 1h; Product distribution / selectivity;
Guidance literature:
Multi-step reaction with 4 steps
1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1.75 h / 0 - 20 °C
2: dmap; triethylamine / dichloromethane / 2 h / 0 - 20 °C
3: OD column / hexane; isopropyl alcohol / Resolution of racemate
4: hydrogen / palladium 10% on activated carbon / methanol / 7 h
With dmap; oxalyl dichloride; hydrogen; triethylamine; palladium 10% on activated carbon; N,N-dimethyl-formamide; In methanol; hexane; dichloromethane; isopropyl alcohol;
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