SS-acetylphenylalanine α-phenylethylamide

Base Information

Chemical Name:SS-acetylphenylalanine α-phenylethylamide
CAS No.:61884-22-8
Molecular Formula:C₁₉H₂₂N₂O₂
Molecular Weight:310.396
Hs Code.:

Synonyms:

Suppliers and Price of SS-acetylphenylalanine α-phenylethylamide

Supply Marketing:

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

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Chemical Property of SS-acetylphenylalanine α-phenylethylamide

Chemical Property:

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MSDS Files:

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Technology Process of SS-acetylphenylalanine α-phenylethylamide

There total 7 articles about SS-acetylphenylalanine α-phenylethylamide 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:

: 2627-86-3
(S)-1-phenyl-ethylamine

: 38879-46-8
(Z)-4-benzylidene-2-methyl-5(4H)-oxazolone

: 61884-22-8
SS-acetylphenylalanine α-phenylethylamide

Guidance literature:: With hydrogen; palladium dichloride;
DOI:10.1007/BF00962000

Reference yield:

: 881-90-3
4-benzylidene-2-methyl-2-oxazolin-5-one

: 2627-86-3
(S)-1-phenyl-ethylamine

: 61884-22-8
SS-acetylphenylalanine α-phenylethylamide

: (R)-2-Acetylamino-3-phenyl-N-((S)-1-phenyl-ethyl)-propionamide

Guidance literature:: With hydrogen; palladium dichloride; In 1,2-dimethoxyethane; Rate constant; Mechanism; Product distribution; excess of diastereomer; effect of educt ratio;
DOI:10.1007/BF00954273

Reference yield:

: 5469-44-3
2-methyl-4-benzyl-4H-oxazolin-5-one

: 2627-86-3
(S)-1-phenyl-ethylamine

: 61884-22-8
SS-acetylphenylalanine α-phenylethylamide

: (R)-2-Acetylamino-3-phenyl-N-((S)-1-phenyl-ethyl)-propionamide

Guidance literature:: In tert-butyl alcohol; at 20 ℃; for 24h; Product distribution; Mechanism; Rate constant; effect of racemization; excess of diastereomer;
DOI:10.1007/BF00954272