(R)-ethyl2-amino-4-phenylbutanoate

Base Information

Chemical Name:(R)-ethyl2-amino-4-phenylbutanoate
CAS No.:124044-66-2
Molecular Formula:C12H17NO2
Molecular Weight:207.272
Hs Code.:
DSSTox Substance ID:DTXSID80424907
Nikkaji Number:J732.378F
Wikidata:Q72482599
Mol file:124044-66-2.mol

Synonyms:124044-66-2;(R)-ethyl2-amino-4-phenylbutanoate;ethyl (2R)-2-amino-4-phenylbutanoate;D-Homophenylalanine ethyl ester;(R)-ethyl 2-amino-4-phenylbutanoate;D-Homophenylalanine ethyl ester;Benzenebutanoic acid, alpha-amino-, ethyl ester, (alphaR)-;SCHEMBL8174213;DTXSID80424907;AKOS015909994;AKOS015933074;EN300-60147

Suppliers and Price of (R)-ethyl2-amino-4-phenylbutanoate

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 11 raw suppliers

Chemical Property of (R)-ethyl2-amino-4-phenylbutanoate

Chemical Property:

Boiling Point:311.4 °C at 760 mmHg
Flash Point:164.8 °C
PSA：52.32000
Density:1.058g/cm³
LogP:2.20990
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:207.125928785
Heavy Atom Count:15
Complexity:188

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C(CCC1=CC=CC=C1)N
Isomeric SMILES:CCOC(=O)[C@@H](CCC1=CC=CC=C1)N

Technology Process of (R)-ethyl2-amino-4-phenylbutanoate

There total 18 articles about (R)-ethyl2-amino-4-phenylbutanoate 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:

Reference yield: 100.0%

: 64-17-5
ethanol

: 1012-05-1
D,L-homophenylalanine

: 46460-23-5,46460-24-6,82830-84-0,124044-66-2
ethyl L-2-amino-4-phenylbutyrate

Guidance literature:: ethanol; D,L-homophenylalanine; With thionyl chloride; Reflux;

With sodium hydrogencarbonate;
DOI:10.1016/j.tetasy.2010.02.011

Reference yield: 89.0%

: 64-17-5
ethanol

: 82795-51-5
D-homophenylalanine

: 124044-66-2
(R)-ethyl 2-amino-4-phenylbutanoate

Guidance literature:: With hydrogenchloride; sodium carbonate;
DOI:10.1002/ardp.19943271111

Reference yield: 72.0%

: 7064-04-2
ethyl 5-phenyl-2-isoxazoline-3-carboxylate

: 46460-23-5,46460-24-6,82830-84-0,124044-66-2
ethyl L-2-amino-4-phenylbutyrate

Guidance literature:: ethyl 5-phenyl-2-isoxazoline-3-carboxylate; With palladium 10% on activated carbon; ammonium formate; In ethanol; for 1h; Reflux;

With hydrogenchloride; zinc; In ethanol; water; at 0 ℃; for 1.5h;
DOI:10.3762/bjoc.14.263