690997-04-7

Basic information

• Product Name: (S)-4-benzyl-2-(9-anthryl)-1,3-oxazoline
• Synonyms: (S)-4-benzyl-2-(9-anthryl)-1,3-oxazoline
• CAS NO: 690997-04-7
• Molecular Weight: 337.421
• Mol File: 690997-04-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-4-benzyl-2-(9-anthryl)-1,3-oxazoline(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-benzyl-2-(9-anthryl)-1,3-oxazoline(690997-04-7)
• EPA Substance Registry System: (S)-4-benzyl-2-(9-anthryl)-1,3-oxazoline(690997-04-7)

Safety Data

• Hazardous Substances Data: 690997-04-7(Hazardous Substances Data)

Upstream product

• 723-62-6 anthracen-9-carboxylic acid 
• 3182-95-4 L-Phenylalaninol 
• 16331-52-5 9-anthracenecarbonyl chloride 
• 690997-08-1 anthracene-9-carboxylic acid (1S-benzyl-2-chloro-ethyl)-amide 

Relevant articles and documents

Bromotriphenylphosphonium salt promoted tandem one-pot cyclization to optically active 2-Aryl-1,3-oxazolines

Optically active 2-aryl-1,3-oxazolines, such as aromatic carbocycles, heterocycle-binding 4-benzyl (or phenyl)-1,3oxazolines and their 5-benzyl (or phenyl)-l,3-oxazoline isomers were successfully prepared through a bromotriphenylphosphonium salt promoted aziridine ring formation and ring opening sequential process involving tandem one pot cyclization of chiral 2-amino-3-phenylpropanol or 2amino-2-phenylethanol with various aromatic acids in toluene at 90 °C in moderate to excellent yields. The mechanism of this tandem process was also substantiated experimentally.