173094-49-0

Basic information

• Product Name: (4S,5S)-4-<(allyloxy)methyl>-2-methyl-5-phenyloxazol-2-ine
• Synonyms: (4S,5S)-4-<(allyloxy)methyl>-2-methyl-5-phenyloxazol-2-ine
• CAS NO: 173094-49-0
• Molecular Weight: 231.294
• Mol File: 173094-49-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4S,5S)-4-<(allyloxy)methyl>-2-methyl-5-phenyloxazol-2-ine(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5S)-4-<(allyloxy)methyl>-2-methyl-5-phenyloxazol-2-ine(173094-49-0)
• EPA Substance Registry System: (4S,5S)-4-<(allyloxy)methyl>-2-methyl-5-phenyloxazol-2-ine(173094-49-0)

Safety Data

• Hazardous Substances Data: 173094-49-0(Hazardous Substances Data)

Upstream product

• 53732-41-5 (4S,5S)-4-Hydroxymethyl-2-methyl-5-phenyl-4,5-dihydro-1,3-oxazole 
• 106-95-6 allyl bromide 

Relevant articles and documents

Synthese d'oxazolines insaturees isomeres a partir d'aminoalcools chiraux en vue du greffage sur silice

Synthesis of unsaturated oxazoline isomers from chiral amino alcohols for bonding to silica.In order to study their enantioselective ability, four chiral unsaturated oxazoline isomers were synthesized from (1S,2S)-2-amino-1-phenylpropane-1,3-diol and (2S,3R)-2-amino-3-hydroxybutanoic acid (S-threonine).A terminal double bond was introduced on these structures in order to be able to graft them onto silica and access chiral stationary phases for chromatography. - Keywords: chiral unsaturated oxazoline; heterocyclization; selective reaction; grafted silica