1668-82-2

Basic information

• Product Name: Oxazolidine, 3,4-dimethyl-5-phenyl-
• CAS NO: 1668-82-2
• Molecular Formula: C11H15NO
• Molecular Weight: 177.246
• Mol File: 1668-82-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Oxazolidine, 3,4-dimethyl-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazolidine, 3,4-dimethyl-5-phenyl-(1668-82-2)
• EPA Substance Registry System: Oxazolidine, 3,4-dimethyl-5-phenyl-(1668-82-2)

Safety Data

• Hazardous Substances Data: 1668-82-2(Hazardous Substances Data)

Upstream product

• 299-42-3 (R,R)-(-)-pseudoephedrine 
• 67-68-5 dimethyl sulfoxide 
• 14746-44-2 methyl-ephedrine N-oxide 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 117371-77-4 1-(R)-2-(S)-methylephedrine N-oxide 
• 100-42-5 styrene 
• 50-00-0 formaldehyd 
• 90-81-3 ephedrine 
• 90-82-4 rac-pseudoephedrine 

Downstream Products

• 67844-53-5 N-formylephedrine 
• 42932-20-7 N-formylmethamphetamine 
• 23582-27-6 3,3,4-trimethyl-5-phenyl-oxazolidinium; iodide 

Relevant articles and documents

STUDY OF THE ASYMMETRIC INDUCTION OF THE 1,3-DIPOLAR CYCLOADDITION OF CHIRAL AZOMETHINE YLIDES WITH UNACTIVATED DOUBLE BONDS

The asymmetric induction of the 1,3-dipolar cycloaddition reaction between nonstabilized azomethine ylides generated by deprotonation of the corresponding tertiary amine N-oxides (1a-f) with a base and various unactivated olefins (2a-c) or dienes (2d-e) h

The Use of the β-Amino-Alcohol-N-Oxide Derivatives in the Synthesis of 2,3 or 4-Alkyl Substituted NH Pyrrolidines

Nonstabilized azomethine ylides generated from the various β-amino alcohols N-oxides 13, 17, 23 and 24 undergo cycloaddition reactions with unactivated alkenes to afford the corresponding pyrrolidines 14a-g, 18a-g, 25 und 27 in moderate to good yields.These compounds are precursors of NH pyrrolidines substituted in position 2, 3 or 4.