55325-49-0

Basic information

• Product Name: (2RS,3SR)-3-Phenylisoserinamide
• CAS NO: 55325-49-0
• Molecular Weight: 180.206
• Mol File: 55325-49-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (2RS,3SR)-3-Phenylisoserinamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2RS,3SR)-3-Phenylisoserinamide(55325-49-0)
• EPA Substance Registry System: (2RS,3SR)-3-Phenylisoserinamide(55325-49-0)

Safety Data

• Hazardous Substances Data: 55325-49-0(Hazardous Substances Data)

Upstream product

• 2272-55-1 ethyl trans-3-phenyl-1-oxirane-2-carboxylate 
• 19190-80-8 cis-methyl 2,3-epoxy-3-phenylpropanoate 
• 121-39-1 ethyl cis-3-phenylglycidate 
• 19190-80-8 methyl trans-3-phenylglycidate 

Downstream Products

• 130517-90-7 Butyric acid (1R,2R)-2-butyrylamino-1-carbamoyl-2-phenyl-ethyl ester 
• 6049-55-4 (±)-anti-3-amino-2-hydroxy-3-phenylpropanoic acid 
• 32981-85-4 syn-(+/-)-2-hydroxy-3-(benzoylamino)-3-phenylpropanoic acid methyl ester 
• 32981-85-4 methyl (2R,3S)-3-benzoylamino-2-hydroxy-3-phenylpropanoate 
• 7309-55-9 N-benzoyl-(2R^*,3S^*)-3-phenylisoserine 

Relevant articles and documents

A practical and stereoselective synthesis of taxol side chain

Apractical and efficient synthesis of taxol C-13 side chain from cheap and easily available starting material is described.

Process for the preparation of (2r,3s)-3-phenylisoserine methyl ester acetate salt

A process for the enantioselective preparation of (2R,3S)-3-phenylisoserine methyl ester acetate salt of formula (I) which is an useful building block for the synthesis of taxane derivatives. The process involves the resolution of racemic threo-phenylisoserine amide and its conversion into (I).

A Practical, Highly Enantioselective Synthesis of the Taxol Side Chain via Asymmetric Catalysis

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