889893-47-4

Basic information

• Product Name: (R)-4-hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate
• Synonyms: (R)-4-hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate
• CAS NO: 889893-47-4
• Molecular Weight: 249.266
• Mol File: 889893-47-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-4-hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-4-hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate(889893-47-4)
• EPA Substance Registry System: (R)-4-hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate(889893-47-4)

Safety Data

• Hazardous Substances Data: 889893-47-4(Hazardous Substances Data)

Upstream product

• 108-05-4 vinyl acetate 
• 62203-32-1 2-phenyl-4(bis-hydroxymethyl)-Δ²-oxazoline 

Downstream Products

• 889893-52-1 (R)-4-(tert-butyldimethylsiloxymethyl)-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate 
• 889893-57-6 methyl (S)-2-benzoyloxymethyl-5-oxopyrrolidine-2-carboxylate 
• 889893-50-9 ethyl (S,E)-3-(4-hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-yl)acrylate 
• 889893-51-0 ethyl (S)-3-(4-hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-yl)propionate 
• 889893-58-7 ethyl (R)-3-(4-hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-yl)propionate 
• 889893-56-5 methyl (S)-4-(2-ethoxycarbonylethyl)-2-phenyl-4,5-dihydrooxazole-4-carboxylate 
• 889893-53-2 (S)-(-)-(4-(tert-butyldimethylsilyloxymethyl)-2-phenyl-4,5-dihydrooxazol-4-yl)methanol 
• 889893-49-6 ethyl (R,E)-3-(4-acetoxymethyl-2-phenyl-4,5-dihydrooxazol-4-yl)acrylate 
• 889893-55-4 ethyl (S)-3-[4-(tert-butyldimethylsiloxymethyl)-2-phenyl-4,5-dihydrooxazol-4-yl]-propionate 
• 889893-54-3 ethyl (S,E)-3-[4-(tert-butyldimethylsiloxymethyl)-2-phenyl-4,5-dihydrooxazol-4-yl]acrylate 

Relevant articles and documents

(R)-4-Hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate: chiral building block for the synthesis of optically active α-substituted α-amino acid derivatives

(R)-4-Hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate was efficiently obtained by lipase-catalyzed asymmetrization of the prochiral diol. (R)-4-Hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate was converted to (R)-2-(hydroxymethyl)g