73697-99-1

Basic information

• Product Name: ((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-(4-methoxy-phenyl)-phenyl-methanol
• CAS NO: 73697-99-1
• Molecular Weight: 403.478
• Mol File: 73697-99-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-(4-methoxy-phenyl)-phenyl-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: ((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-(4-methoxy-phenyl)-phenyl-methanol(73697-99-1)
• EPA Substance Registry System: ((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-(4-methoxy-phenyl)-phenyl-methanol(73697-99-1)

Safety Data

• Hazardous Substances Data: 73697-99-1(Hazardous Substances Data)

Upstream product

• 63007-15-8 trans-(4S,5S)-2-benzoyl-4-(methoxymethyl)-5-phenyl-2-oxazoline 
• 14774-77-7 p-methoxyphenyllithium 
• 58635-82-8 (S,S)-2-benzyl-4-methoxymethyl-5-phenyl-2-oxazoline 

Downstream Products

• 73698-07-4 (S)-4-methoxy-benzilic acid 
• 4237-50-7 (R)-2-hydroxy-2-(4-methoxyphenyl)-2-phenylacetic acid 

Relevant articles and documents

Asymmetric Addition of Organometallics to Chiral Ketooxazolines. Preparation of Enantiomerically Enriched α-Hydroxy Acids

Addition of Grignard and organolithium reagents to chiral α-ketooxazolines results in α-substituted α-hydroxyoxazoline derivatives which on hydrolytic removal of the chiral auxiliary groups give rise to α-substituted α-hydroxy acids in 30-87 percent enantiomeric excess (ee).Studies on the various parameters (solvents, temperature, substituents) were undertaken to reach optimum asymmetric induction.