(S)-Methyl 2-amino-3-(4-methoxyphenyl)propanoate hydrochloride

Base Information

• Chemical Name: (S)-Methyl 2-amino-3-(4-methoxyphenyl)propanoate hydrochloride
• CAS No.: 7479-01-8
• Molecular Formula: C11H15NO3
• Molecular Weight: 245.706
• NSC Number: 401573

Synonyms:64657-63-2;L-Tyrosine, O-methyl-, methyl ester, hydrochloride;O-Methyl-L-tyrosine methyl ester HCl;7479-01-8;Methyl 2-amino-3-(4-methoxyphenyl)propanoate hydrochloride;(S)-Methyl 2-amino-3-(4-methoxyphenyl)propanoate hydrochloride;methyl 2-amino-3-(4-methoxyphenyl)propanoate;hydrochloride;SCHEMBL7301098;NSC401573;NSC-401573;F97079;4-METHOXY-DL-PHENYLALANINE METHYL ESTER HCL

Chemical Property of (S)-Methyl 2-amino-3-(4-methoxyphenyl)propanoate hydrochloride

Chemical Property:

• Vapor Pressure: 0.000659mmHg at 25°C
• Boiling Point: 309°Cat760mmHg
• Flash Point: 127.5°C
• Density: 1.12g/cm³
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 245.0818711
• Heavy Atom Count: 16
• Complexity: 200

Purity/Quality:

97% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)CC(C(=O)OC)N.Cl

Technology Process of (S)-Methyl 2-amino-3-(4-methoxyphenyl)propanoate hydrochloride

There total 15 articles about (S)-Methyl 2-amino-3-(4-methoxyphenyl)propanoate hydrochloride 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: 98.0%

(S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoate (94790-24-6) → O-methyl-L-tyrosine methyl ester hydrochloride (7479-01-8)

Guidance literature:

With acetyl chloride; In methanol; at 0 - 20 ℃; for 6h;

DOI:10.1016/j.ejmech.2016.09.002

Reference yield: 95.0%

methanol (67-56-1) + O-methyl-N-tert-butoxycarbonyl-L-tyrosine (53267-93-9) → O-methyl-L-tyrosine methyl ester hydrochloride (7479-01-8)

Guidance literature:

With chloro-trimethyl-silane; at 20 ℃; for 18h;

DOI:10.1021/jo990311w

Reference yield: 84.0%

→ O-methyl-L-tyrosine methyl ester hydrochloride (7479-01-8)

Guidance literature:

upstream raw materials:

methanol

O-methyl tyrosine

p-methoxybenzyl chloride

2-amino-3-(4-methoxyphenyl)propionic acid hydrochloride

Downstream raw materials:

DL-2-Amino-1,1,3-tris(4-methoxyphenyl)-1-propanol

DL-1-Azido-1,1,3-tris(4-methoxyphenyl)-2-propanamine

C₁₄H₁₅NO₄

butyl 2-acetylamino-3-(4-methoxyphenyl)propanoate

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