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Pentanoic acid, 2-methyl-3-oxo-, phenylmethyl ester

Base Information Edit
  • Chemical Name:Pentanoic acid, 2-methyl-3-oxo-, phenylmethyl ester
  • CAS No.:162662-03-5
  • Molecular Formula:C13H16O3
  • Molecular Weight:220.268
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30433786
  • Nikkaji Number:J655.258G
  • Mol file:162662-03-5.mol
Pentanoic acid, 2-methyl-3-oxo-, phenylmethyl ester

Synonyms:Pentanoic acid, 2-methyl-3-oxo-, phenylmethyl ester;162662-03-5;SCHEMBL9881032;DTXSID30433786;2-Methyl-3-oxovaleric acid benzyl ester

Suppliers and Price of Pentanoic acid, 2-methyl-3-oxo-, phenylmethyl ester
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 Pentanoic acid, 2-methyl-3-oxo-, phenylmethyl ester Edit
Chemical Property:
  • XLogP3:2.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:6
  • Exact Mass:220.109944368
  • Heavy Atom Count:16
  • Complexity:242
Purity/Quality:

99.90% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC(=O)C(C)C(=O)OCC1=CC=CC=C1
Technology Process of Pentanoic acid, 2-methyl-3-oxo-, phenylmethyl ester

There total 5 articles about Pentanoic acid, 2-methyl-3-oxo-, phenylmethyl ester 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 potassium tert-butylate; at 120 ℃; for 1h;
DOI:10.1016/S0040-4039(01)01562-3
Guidance literature:
With lithium diisopropyl amide; In tetrahydrofuran; hexane; at -78 ℃; for 2h; Product distribution; Mechanism; various reaction conditions;
Guidance literature:
With trifluoroacetic acid; In acetonitrile; at 0 - 20 ℃; for 24h; Inert atmosphere;
DOI:10.1002/hlca.201100375
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