L-Methionine, N-(2-amino-3-phenylpropyl)-, methyl ester, (S)-

Base Information

Chemical Name:L-Methionine, N-(2-amino-3-phenylpropyl)-, methyl ester, (S)-
CAS No.:158861-44-0
Molecular Formula:C₁₅H₂₄N₂O₂S
Molecular Weight:296.434
Hs Code.:
DSSTox Substance ID:DTXSID401181516

Synonyms:SCHEMBL9555078;DTXSID401181516;L-Methionine, N-(2-amino-3-phenylpropyl)-, methyl ester, (S)-;158861-44-0

Suppliers and Price of L-Methionine, N-(2-amino-3-phenylpropyl)-, methyl ester, (S)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of L-Methionine, N-(2-amino-3-phenylpropyl)-, methyl ester, (S)-

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:10
Exact Mass:296.15584919
Heavy Atom Count:20
Complexity:271

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)C(CCSC)NCC(CC1=CC=CC=C1)N
Isomeric SMILES:COC(=O)[C@H](CCSC)NC[C@H](CC1=CC=CC=C1)N

Technology Process of L-Methionine, N-(2-amino-3-phenylpropyl)-, methyl ester, (S)-

There total 3 articles about L-Methionine, N-(2-amino-3-phenylpropyl)-, methyl ester, (S)- 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%

: 158861-43-9
N-<2-(S)-<(tert-butoxycarbonyl)amino>-3-phenylpropyl>-methionine methyl ester

: 158861-44-0
N-(2-(S)-amino-3-phenylpropyl)methionine methyl ester

Guidance literature:: With hydrogenchloride; In ethyl acetate; at -20 ℃; for 0.5h;
DOI:10.1021/jm00032a004

Reference yield:

: 72155-45-4
Boc-L-phenylalaninal

: 158861-44-0
N-(2-(S)-amino-3-phenylpropyl)methionine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / AcOH, sodium cyanoborohydride / methanol / 2 h

2: 100 percent / HCl (g) / ethyl acetate / 0.5 h / -20 °C

With hydrogenchloride; sodium cyanoborohydride; acetic acid; In methanol; ethyl acetate;
DOI:10.1021/jm00032a004

Reference yield:

: 2491-18-1
(S)-methyl 2-amino-4-(methylthio)butanoate hydrochloride

: 158861-44-0
N-(2-(S)-amino-3-phenylpropyl)methionine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / AcOH, sodium cyanoborohydride / methanol / 2 h

2: 100 percent / HCl (g) / ethyl acetate / 0.5 h / -20 °C

With hydrogenchloride; sodium cyanoborohydride; acetic acid; In methanol; ethyl acetate;
DOI:10.1021/jm00032a004