503178-23-2

Basic information

• Product Name: 3-Benzoylamino-2-hydroxy-3-phenyl-propionic acid methyl ester
• Synonyms: 3-Benzoylamino-2-hydroxy-3-phenyl-propionic acid methyl ester
• CAS NO: 503178-23-2
• Molecular Weight: 299.326
• Mol File: 503178-23-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-Benzoylamino-2-hydroxy-3-phenyl-propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Benzoylamino-2-hydroxy-3-phenyl-propionic acid methyl ester(503178-23-2)
• EPA Substance Registry System: 3-Benzoylamino-2-hydroxy-3-phenyl-propionic acid methyl ester(503178-23-2)

Safety Data

• Hazardous Substances Data: 503178-23-2(Hazardous Substances Data)

Upstream product

• 33069-62-4 Taxol 
• 67-56-1 methanol 
• 98-88-4 benzoyl chloride 
• 51608-62-9 (E)-N-benzylidenebenzamide 

Downstream Products

• 151764-53-3 (2R,3R)-(-)-2-hydroxy-3-(benzoylamino)-3-phenylpropanoic acid methyl ester 
• 161060-39-5 (2S,3S)-2-acetyloxy-3-(benzoylamino)-3-phenylpropanoic acid methyl ester 
• 144541-45-7 methyl (2S,3S)-3-benzoylamino-2-hydroxy-3-phenylpropanoate 

Relevant articles and documents

A mild and efficient approach for the deprotection of silyl ethers by sodium periodate

A mild and efficient method for the deprotection of silyl ethers is reported. The most often used silyl protecting groups, such as TBDMS, TIPS, TMS, TES, TIBS, TPS can be cleaved by NaIO4 furnishing the corresponding alcohol in high yields. This method can be used for a wide range of substrates.

Chiral Auxiliary-Mediated Asymmetric Induction in a Thermal Inverse Electron Demand Hetero-Diels-Alder Reaction. Enantioselective Synthesis of the Taxol A-Ring Side Chain

Chiral auxiliary-modified ketene acetal 5g and N-benzoylbenzaldimine (4) engage in an endo and ?-facially selective thermal inverse electron demand hetero-Diels-Alder reaction that is the key step in a synthesis of enantiomerically pure taxol A-ring side-chain methyl ester 9.