70546-93-9

Basic information

• Product Name: N-[2-methoxy-2-(4-methoxyphenyl)ethyl]-3-phenyl-2-propenamide
• CAS NO: 70546-93-9
• Molecular Weight: 311.381
• Mol File: 70546-93-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-[2-methoxy-2-(4-methoxyphenyl)ethyl]-3-phenyl-2-propenamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-methoxy-2-(4-methoxyphenyl)ethyl]-3-phenyl-2-propenamide(70546-93-9)
• EPA Substance Registry System: N-[2-methoxy-2-(4-methoxyphenyl)ethyl]-3-phenyl-2-propenamide(70546-93-9)

Safety Data

• Hazardous Substances Data: 70546-93-9(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 1122469-32-2 (+)-(5S)-2-(trans-styryl)-5-(4-methoxyphenyl)-Δ2-oxazoline 
• 31367-42-7 2-(p-methoxyphenyl)-2-methoxyethylamine 
• 102-92-1 cinnamoyl chloride 
• 637-69-4 4-Methoxystyrene 

Relevant articles and documents

Direct catalytic synthesis of unprotected 2-amino-1-phenylethanols from alkenes by using iron(II) phthalocyanine

Aryl-substituted amino alcohols are privileged scaffolds in medicinal chemistry and natural products. Herein, we report that an exceptionally simple and inexpensive FeII complex efficiently catalyzes the direct transformation of simple alkenes into unprotected amino alcohols in good yield and perfect regioselectivity. This new catalytic method was applied in the expedient synthesis of bioactive molecules and could be extended to aminoetherification.