(S)-(+)-2-Amino-N-methyl-3-phenyl-propionamide hydrochloride

Base Information

• Chemical Name: (S)-(+)-2-Amino-N-methyl-3-phenyl-propionamide hydrochloride
• CAS No.: 17186-56-0
• Molecular Formula: C₁₀H₁₄N₂O*ClH
• Molecular Weight: 214.695
• European Community (EC) Number: 622-000-5
• Mol file: 17186-56-0.mol

Synonyms:17186-56-0;(S)-2-amino-N-methyl-3-phenylpropanamide hydrochloride;(S)-(+)-2-Amino-N-methyl-3-phenyl-propionamide hydrochloride;L-phenylalanine methylamide hydrochloride;C10H15ClN2O;UDXSBRWDLXGZIC-FVGYRXGTSA-N;H-Phe-NHMe.HCl;SCHEMBL1262434;AKOS025405043;N-methyl-L-phenylalanine amide hydrochloride;CS-0324203;E79015;(S)-alpha-Amino-N-methyl-benzenepropanamide HCl;(S)-2-amino-N-methyl-3-phenylpropanamidehydrochloride;(2S)-Amino-N-methyl-3-phenyl-propionamide hydrochloride;(2S)-2-AMINO-N-METHYL-3-PHENYLPROPANAMIDE HYDROCHLORIDE;(S)-(+)-2-Amino-N-methyl-3-phenyl-propionamide hydrochloride, >=97.0%

Chemical Property of (S)-(+)-2-Amino-N-methyl-3-phenyl-propionamide hydrochloride

Chemical Property:

• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 214.0872908
• Heavy Atom Count: 14
• Complexity: 164

Purity/Quality:

97% ^*data from raw suppliers

(S)-(+)-2-Amino-N-methyl-3-phenyl-propionamide hydrochloride ≥97.0% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): 4022019
• Hazard Codes: Xi
• Statements: 43
• Safety Statements: 36/37

MSDS Files:

Useful:

• Canonical SMILES: CNC(=O)C(CC1=CC=CC=C1)N.Cl
• Isomeric SMILES: CNC(=O)[C@H](CC1=CC=CC=C1)N.Cl

Technology Process of (S)-(+)-2-Amino-N-methyl-3-phenyl-propionamide hydrochloride

There total 8 articles about (S)-(+)-2-Amino-N-methyl-3-phenyl-propionamide 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: 100.0%

N-(t-butoxycarbonyl)-L-phenylalanine methylamide (109522-21-6) → L-phenylalanine methylamide hydrochloride (17186-56-0,111321-55-2)

Guidance literature:

With hydrogenchloride; In 1,4-dioxane; methanol; for 4h; Ambient temperature;

DOI:10.1021/jm970494j

Reference yield: 89.0%

N-(t-butoxycarbonyl)-L-phenylalanine methylamide (109522-21-6) → H-L-Phe-NHMe*2HCl (17186-56-0,111321-55-2)

Guidance literature:

With hydrogenchloride; for 2h; ice-chilled;

Reference yield:

→ N-t-butoxycarbonyl-L-phenylalanine 4-nitrophenyl ester (7535-56-0) + L-phenylalanine methylamide hydrochloride (17186-56-0,111321-55-2)

Guidance literature:

upstream raw materials:

methyl (2S)-2-amino-3-phenylpropanoate hydrochloride

methylamine

N-(t-butoxycarbonyl)-L-phenylalanine methylamide

N-tert-butoxycarbonyl-L-phenylalanine

Downstream raw materials:

(R)-5-Methyl-3-((S)-1-methylcarbamoyl-2-phenyl-ethylcarbamoyl)-hexanoic acid methyl ester

(2S,5S)-5-benzyl-3-methyl-2-phenylimidazolidin-4-one

5-benzyl-3-methyl-2-phenylimidazolidin-4-one

[(1S,2R,3S,4S)-3-((S)-1-Methylcarbamoyl-2-phenyl-ethylcarbamoyl)-1,2,3,4-tetrahydro-1,4-methano-naphthalen-2-yl]-carbamic acid methyl ester

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