624732-06-5

Basic information

• Product Name: (1R,2S)-2-(methyl-{[(1R,2R)-2-phenylcyclopropyl](methyl)}amino)-1-phenylpropan-1-ol
• Synonyms: (1R,2S)-2-(methyl-{[(1R,2R)-2-phenylcyclopropyl](methyl)}amino)-1-phenylpropan-1-ol
• CAS NO: 624732-06-5
• Molecular Weight: 295.425
• Mol File: 624732-06-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1R,2S)-2-(methyl-{[(1R,2R)-2-phenylcyclopropyl](methyl)}amino)-1-phenylpropan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S)-2-(methyl-{[(1R,2R)-2-phenylcyclopropyl](methyl)}amino)-1-phenylpropan-1-ol(624732-06-5)
• EPA Substance Registry System: (1R,2S)-2-(methyl-{[(1R,2R)-2-phenylcyclopropyl](methyl)}amino)-1-phenylpropan-1-ol(624732-06-5)

Safety Data

• Hazardous Substances Data: 624732-06-5(Hazardous Substances Data)

Upstream product

• 4392-24-9 Cinnamyl bromide 
• 299-42-3 ephedrine 
• 75-11-6 diiodomethane 
• 90-86-8 (1R,2S)-2-{methyl-[(E)-3-phenyl-2-propenyl]amino}-1-phenylpropan-1-ol 

Downstream Products

• 624732-11-2 2-phenyl-1-(N,N-dimethylamino)methyl-cyclopropane 

Relevant articles and documents

Highly Diastereoselective Simmons-Smith Cyclopropanation of Allylic Amines

(Equation presented) Cyclopropanation of allylic tertiary amines using the Simmons-Smith reagent has been achieved by employing chelating groups in close proximity to the amine. The chelating groups promote cyclopropanation at the expense of N-ylide formation. Using pseudoephedrine as the chelating group, high diastereoselectivity is observed.