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3-Oxazolidinecarboxylic acid, 4-ethyl-5-oxo-, phenylmethyl ester, (R)-

Base Information
  • Chemical Name:3-Oxazolidinecarboxylic acid, 4-ethyl-5-oxo-, phenylmethyl ester, (R)-
  • CAS No.:189878-68-0
  • Molecular Formula:C13H15NO4
  • Molecular Weight:249.266
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70456691
  • Wikidata:Q82279247
  • Mol file:189878-68-0.mol
3-Oxazolidinecarboxylic acid, 4-ethyl-5-oxo-, phenylmethyl ester, (R)-

Synonyms:189878-68-0;(R)-Benzyl 4-ethyl-5-oxooxazolidine-3-carboxylate;3-Oxazolidinecarboxylic acid, 4-ethyl-5-oxo-, phenylmethyl ester, (R)-;DTXSID70456691

Suppliers and Price of 3-Oxazolidinecarboxylic acid, 4-ethyl-5-oxo-, phenylmethyl ester, (R)-
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
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of 3-Oxazolidinecarboxylic acid, 4-ethyl-5-oxo-, phenylmethyl ester, (R)-
Chemical Property:
  • XLogP3:2.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:249.10010796
  • Heavy Atom Count:18
  • Complexity:312
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1C(=O)OCN1C(=O)OCC2=CC=CC=C2
  • Isomeric SMILES:CC[C@@H]1C(=O)OCN1C(=O)OCC2=CC=CC=C2
Technology Process of 3-Oxazolidinecarboxylic acid, 4-ethyl-5-oxo-, phenylmethyl ester, (R)-

There total 1 articles about 3-Oxazolidinecarboxylic acid, 4-ethyl-5-oxo-, phenylmethyl ester, (R)- 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 sodium hydrogencarbonate; acetic acid; Yield given. Multistep reaction; 1.) toluene, 40 deg C, 24 h, 2.) EtOH, 65 deg C, 2 h;
DOI:10.1080/00304949709355181
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