1380547-26-1

Basic information

• Product Name: methyl 3-((R)-5-oxo-4-((R)-3-oxo-1-phenylbutyl)-2-phenyl-4,5-dihydrooxazol-4-yl)propanoate
• Synonyms: methyl 3-((R)-5-oxo-4-((R)-3-oxo-1-phenylbutyl)-2-phenyl-4,5-dihydrooxazol-4-yl)propanoate
• CAS NO: 1380547-26-1
• Molecular Weight: 393.439
• Mol File: 1380547-26-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 3-((R)-5-oxo-4-((R)-3-oxo-1-phenylbutyl)-2-phenyl-4,5-dihydrooxazol-4-yl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-((R)-5-oxo-4-((R)-3-oxo-1-phenylbutyl)-2-phenyl-4,5-dihydrooxazol-4-yl)propanoate(1380547-26-1)
• EPA Substance Registry System: methyl 3-((R)-5-oxo-4-((R)-3-oxo-1-phenylbutyl)-2-phenyl-4,5-dihydrooxazol-4-yl)propanoate(1380547-26-1)

Safety Data

• Hazardous Substances Data: 1380547-26-1(Hazardous Substances Data)

Upstream product

• 1499-55-4 DL-glutamic acid-5-methyl ester 
• 93-97-0 benzoic acid anhydride 
• 1896-62-4 (E)-benzalacetone 

Downstream Products

• 1380547-37-4 (R)-2-benzamido-2-((R)-3-oxo-1-phenylbutyl)pentanedioic acid 
• 1380547-38-5 (R)-dimethyl 2-benzamido-2-((R)-3-oxo-1-phenylbutyl)pentanedioate 

Relevant articles and documents

Catalytic asymmetric synthesis of functionalized α,α- disubstituted α-amino acid derivatives from racemic unprotected α-amino acids via in-situ generated azlactones

Masked and activated highly enantioenriched α,α-disubstituted α-amino acids with an additional adjacent stereocenter were formed by a tandem reaction involving five steps using racemic unprotected amino acid substrates. Key step is the 1,4-addition of in-situ generated azlactones to a broad number of enones. The products of this step-economic route can, e.g., be useful for a divergent and rapid access to biologically interesting unnatural glutamic acid derivatives. Copyright