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Ethyl 2-(phenylamino)propanoate

Base Information
  • Chemical Name:Ethyl 2-(phenylamino)propanoate
  • CAS No.:54860-84-3
  • Molecular Formula:C11H15 N O2
  • Molecular Weight:193.246
  • Hs Code.:
  • NSC Number:165819
  • DSSTox Substance ID:DTXSID50304449
  • Nikkaji Number:J2.116.845I
Ethyl 2-(phenylamino)propanoate

Synonyms:Ethyl 2-(phenylamino)propanoate;54860-84-3;Alanine, N-phenyl-, ethyl ester;88912-03-2;Ethyl N-phenylalaninate;ethyl 2-anilinopropanoate;DL-Phenylalanine, ethyl ester;SCHEMBL8031605;DTXSID50304449;FMFDWCAQDWISCD-UHFFFAOYSA-N;MFCD00026880;NSC165819;AKOS010217600;NSC-165819;BB 0301289;EN300-24217173

Suppliers and Price of Ethyl 2-(phenylamino)propanoate
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 4 raw suppliers
Chemical Property of Ethyl 2-(phenylamino)propanoate
Chemical Property:
  • Vapor Pressure:0.003mmHg at 25°C 
  • Boiling Point:284.3°Cat760mmHg 
  • Flash Point:125.7°C 
  • Density:1.08g/cm3 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:193.110278721
  • Heavy Atom Count:14
  • Complexity:176
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)C(C)NC1=CC=CC=C1
Technology Process of Ethyl 2-(phenylamino)propanoate

There total 6 articles about Ethyl 2-(phenylamino)propanoate 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 tris-(dibenzylideneacetone)dipalladium(0); (S,E)-N-benzhydryl-2-(N,N'-dicyclohexylcarbamimidoyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxamide; In dichloromethane; at 35 ℃; for 5h; enantioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201308501
Guidance literature:
L-2-aminobutyric acid ethyl ester hydrochloride; With potassium carbonate; In ethanol; at 20 ℃; for 1h; Inert atmosphere;
2-iodocyclohex-2-en-1-one; With toluene-4-sulfonic acid; In ethanol; at 75 ℃; for 6h; Inert atmosphere;
DOI:10.1002/ejoc.201201263
Guidance literature:
With C32H30N4O4; copper(l) chloride; In dichloromethane; at 0 ℃; for 8h; optical yield given as %ee; enantioselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1002/anie.201001686
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