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Ethyl L-phenylalanate

Base Information Edit
  • Chemical Name:Ethyl L-phenylalanate
  • CAS No.:3081-24-1
  • Molecular Formula:C11H15 N O2
  • Molecular Weight:193.246
  • Hs Code.:
  • European Community (EC) Number:221-378-5
  • UNII:26O5DCZ9XV
  • DSSTox Substance ID:DTXSID20184816
  • Nikkaji Number:J103.965B
  • ChEMBL ID:CHEMBL1221903
  • Mol file:3081-24-1.mol
Ethyl L-phenylalanate

Synonyms:L-phenylalanine ethylester;phenylalanine ethylester

Suppliers and Price of Ethyl L-phenylalanate
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 4 raw suppliers
Chemical Property of Ethyl L-phenylalanate Edit
Chemical Property:
  • Melting Point:136°C 
  • Refractive Index:1.5041 (estimate) 
  • Boiling Point:281.3°Cat760mmHg 
  • PKA:7.29±0.33(Predicted) 
  • Flash Point:140.3°C 
  • PSA:52.32000 
  • Density:1.077g/cm3 
  • LogP:1.81980 
  • XLogP3:1.5
  • 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:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)C(CC1=CC=CC=C1)N
  • Isomeric SMILES:CCOC(=O)[C@H](CC1=CC=CC=C1)N
Technology Process of Ethyl L-phenylalanate

There total 78 articles about Ethyl L-phenylalanate 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 hydrogenchloride; at 60 ℃; for 1h; prototype reaction (other amino acids and peptides);
DOI:10.1021/ac00277a056
Guidance literature:
With Thiosalicylic acid; 1,4-di(diphenylphosphino)-butane; bis(dibenzylideneacetone)-palladium(0); In tetrahydrofuran; at 60 ℃; for 0.25h;
DOI:10.1016/0040-4039(95)00003-U

Reference yield: 73.0%

Guidance literature:
C32H36N2O4; With water; hydrogenchloride; In water; ethyl acetate; toluene; at 20 ℃; for 1h;
With sodium carbonate; In water;
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