71982-21-3

Basic information

• Product Name: Benzenepropanamine, N-ethyl-N-phenyl-
• CAS NO: 71982-21-3
• Molecular Formula: C17H21N
• Molecular Weight: 239.36
• Mol File: 71982-21-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenepropanamine, N-ethyl-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanamine, N-ethyl-N-phenyl-(71982-21-3)
• EPA Substance Registry System: Benzenepropanamine, N-ethyl-N-phenyl-(71982-21-3)

Safety Data

• Hazardous Substances Data: 71982-21-3(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 128502-28-3 N-ethyl-N-[(2E)-3-phenylprop-2-en-1-yl]aniline 
• 60-29-7 diethyl ether 
• 3271-81-6 hydrocinnamanilide 
• 103-69-5 N-ethyl-N-phenylamine 
• 104-54-1 3-Phenylpropenol 
• 104-53-0 3-phenyl-propionaldehyde 
• 122-97-4 3-Phenyl-1-propanol 
• 104-55-2 3-phenyl-propenal 
• 100-42-5 styrene 
• 201230-82-2 carbon monoxide 
• 4119-41-9 1-iodo-3-phenylpropan 

Relevant articles and documents

Carboxamides as N-Alkylating Reagents of Secondary Amines in Indium-Catalyzed Reductive Amination with a Hydrosilane

A method for the catalytic reductive N-alkylation of amines by using secondary amides as the alkyl source was developed. A versatile type of carboxamide functioned as an N-alkylation reagent in the presence of an indium(III) catalyst and a hydrosilane to provide alkylated tertiary amines efficiently. This amide-based catalytic N-alkylation strategy is considered to be a highly useful protocol to access unsymmetrical tertiary amines.

Ruthenium-catalyzed reductive amination of allylic alcohols

Straighforward access to various saturated amines from allylic alcohols and isostructural mixture can now be achieved in the presence of arene ruthenium catalyst featuring phosphinesulfonate ligand and a hydrogen donor.