157722-43-5

Basic information

• Product Name: (2R,3S)-3-Benzoylamino-3-phenyl-2-trimethylsilanyloxy-propionic acid methyl ester
• Synonyms: (2R,3S)-3-Benzoylamino-3-phenyl-2-trimethylsilanyloxy-propionic acid methyl ester
• CAS NO: 157722-43-5
• Molecular Weight: 371.508
• Mol File: 157722-43-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3S)-3-Benzoylamino-3-phenyl-2-trimethylsilanyloxy-propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-3-Benzoylamino-3-phenyl-2-trimethylsilanyloxy-propionic acid methyl ester(157722-43-5)
• EPA Substance Registry System: (2R,3S)-3-Benzoylamino-3-phenyl-2-trimethylsilanyloxy-propionic acid methyl ester(157722-43-5)

Safety Data

• Hazardous Substances Data: 157722-43-5(Hazardous Substances Data)

Upstream product

• 5321-31-3 phenylglycidylchloride hydrochloride 
• 157722-41-3 methyl 3-amino-2-keto-3-phenylpropionate 
• 157722-40-2 (S)-3-Amino-2-oxo-3-phenyl-propionitrile 
• 157240-36-3 (2R,3S)-3-phenylisoserine methyl ester 
• 2935-35-5 (S)-2-phenylglycine 
• 98-88-4 benzoyl chloride 
• 157722-42-4 (2R,3S)-3-Amino-3-phenyl-2-trimethylsilanyloxy-propionic acid methyl ester 

Downstream Products

• 32981-85-4 methyl (2R,3S)-3-benzoylamino-2-hydroxy-3-phenylpropanoate 

Relevant articles and documents

Application of Yeast-Catalyzed Reductions to Synthesis of (2R,3S)-Phenylisoserine

A simple synthesis of (2R,3S)-phenylisoserine, a precursor of the C-13 side chain of Taxol (paclitaxel), utilising yeast-catalyzed reduction to generate a second chiral centre is reported.This short enantioselective series of transformations can be readily adapted to large scale production of a variety of N-substituted paclitaxel analogues.