875470-19-2

Basic information

• Product Name: N-(4-methoxyphenyl)-α-methyl-1-naphthalenemethanamine
• CAS NO: 875470-19-2
• Molecular Weight: 277.366
• Mol File: 875470-19-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(4-methoxyphenyl)-α-methyl-1-naphthalenemethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methoxyphenyl)-α-methyl-1-naphthalenemethanamine(875470-19-2)
• EPA Substance Registry System: N-(4-methoxyphenyl)-α-methyl-1-naphthalenemethanamine(875470-19-2)

Safety Data

• Hazardous Substances Data: 875470-19-2(Hazardous Substances Data)

Upstream product

• 941-98-0 1'-naphthacetophenone 
• 104-94-9 4-methoxy-aniline 
• 880647-71-2 N-(4-methoxy-phenyl)-4-methyl-N-(1-naphthalen-1-yl-ethyl)-benzenesulfonamide 
• 1150-26-1 N-(4-Methoxy-phenyl)-4-methyl-benzenesulfonamide 
• 57605-95-5 1-(1-naphthyl)ethanol 

Downstream Products

• 880647-72-3 C₁₉H₁₈N₂O₂ 
• 880647-73-4 N-(4-methoxy-phenyl)-N-(1-naphthalen-1-yl-ethyl)-hydrazine 

Relevant articles and documents

Oxidative Kinetic Resolution of Acyclic Amines Based on Equilibrium Control

An oxidative kinetic resolution of racemic acyclic amines was developed using an imine derivative as the resolving reagent and chiral phosphoric acid as the catalyst to give enantiomers in good yields with high to excellent enantioselectivities. The key t

Diphenylphosphanylsulfoximines as ligands in iridium-catalyzed asymmetric imine hydrogenations

(Chemical Equation Presented) Easily accessible phosphine-substituted sulfoximines 2 have been applied in Ir-catalyzed asymmetric hydrogenations of acylic N-arylated imines 1. The amines 3 are formed under mild conditions in high yields with excellent ee