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Ethyl N-benzyl-N-methyloxamate

Base Information
  • Chemical Name:Ethyl N-benzyl-N-methyloxamate
  • CAS No.:128429-34-5
  • Molecular Formula:C12H15 N O3
  • Molecular Weight:221.256
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00155882
  • Nikkaji Number:J292.255J
  • Wikidata:Q83023871
  • Mol file:128429-34-5.mol
Ethyl N-benzyl-N-methyloxamate

Synonyms:EBMO;ethyl N-benzyl-N-methyloxamate;ethyl N-N-benzyl-methyl-oxamate

Suppliers and Price of Ethyl N-benzyl-N-methyloxamate
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 3 raw suppliers
Chemical Property of Ethyl N-benzyl-N-methyloxamate
Chemical Property:
  • Vapor Pressure:0.000331mmHg at 25°C 
  • Boiling Point:319.8°Cat760mmHg 
  • Flash Point:147.2°C 
  • PSA:46.61000 
  • Density:1.128g/cm3 
  • LogP:1.20810 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:221.10519334
  • Heavy Atom Count:16
  • Complexity:247
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)C(=O)N(C)CC1=CC=CC=C1
Technology Process of Ethyl N-benzyl-N-methyloxamate

There total 3 articles about Ethyl N-benzyl-N-methyloxamate 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 pyridine; In dichloromethane; for 5h; Ambient temperature;
DOI:10.1021/jm00057a009
Guidance literature:
With palladium 10% on activated carbon; oxygen; tetra-(n-butyl)ammonium iodide; at 60 ℃; for 2h; under 5320.36 Torr; Autoclave;
DOI:10.1021/jo401038e
Guidance literature:
In acetonitrile; at 20 ℃; for 12h; Sealed tube; Combinatorial reaction / High throughput screening (HTS);
DOI:10.1002/ejoc.201501579
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