17153-00-3

Basic information

• Product Name: 5-acetyloxy-4-methyl-2-phenyloxazole
• Synonyms: 5-acetyloxy-4-methyl-2-phenyloxazole
• CAS NO: 17153-00-3
• Molecular Weight: 217.224
• Mol File: 17153-00-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5-acetyloxy-4-methyl-2-phenyloxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-acetyloxy-4-methyl-2-phenyloxazole(17153-00-3)
• EPA Substance Registry System: 5-acetyloxy-4-methyl-2-phenyloxazole(17153-00-3)

Safety Data

• Hazardous Substances Data: 17153-00-3(Hazardous Substances Data)

Upstream product

• 51127-13-0 2-phenyl-4-methyl-4H-oxazolin-5-one 
• 75-36-5 acetyl chloride 

Downstream Products

• 17153-02-5 rac-4-acetyl-4-methyl-2-phenyloxazol-5-one 
• 1213233-72-7 isopropyl (R,R)-2-benzoylamino-3-hydroxy-2-methylbutyrate 
• 1213233-82-9 (4S,5R)-4-isopropoxycarbonyl-4,5-dimethyl-2-phenyl-1,3-oxazoline 
• 1213233-80-7 (4R,5S)-4-isopropoxycarbonyl-4,5-dimethyl-2-phenyl-1,3-oxazoline 
• 1213233-69-2 isopropyl (S,S)-2-benzoylamino-3-hydroxy-2-methylbutyrate 
• 1213234-70-8 isopropyl (R)-2-benzoylamino-2-methyl-3-oxobutyrate 
• 1213233-44-3 isopropyl (S)-2-benzoylamino-2-methyl-3-oxobutyrate 
• 1031207-95-0 rac-2-benzoylamino-2-methyl-3-oxobutyric acid isopropyl ester 
• 21944-50-3 2-Benzamino-2-methyl-acetessigsaeure-benzylamid 
• 18227-62-8 (+/-)-2-benzamido-3-butanone 

Relevant articles and documents

Novel catalytic synthetic route to protected α-methyl threonine and the first asymmetric acetyl migration in a steglich rearrangement reaction

A short synthetic route to protected α-methyl threonine 5 as a representative example for (protected) α-methylated α-amino-β- hydroxy acids bearing a stereogenic quaternary carbon center in α-position was developed. This multistep synthesis is based on th