324025-11-8

Basic information

• Product Name: Benzenepropanamine, N-(4-methoxyphenyl)-a-methyl-
• CAS NO: 324025-11-8
• Molecular Formula: C17H21NO
• Molecular Weight: 255.36
• Mol File: 324025-11-8.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: Benzenepropanamine, N-(4-methoxyphenyl)-a-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanamine, N-(4-methoxyphenyl)-a-methyl-(324025-11-8)
• EPA Substance Registry System: Benzenepropanamine, N-(4-methoxyphenyl)-a-methyl-(324025-11-8)

Safety Data

• Hazardous Substances Data: 324025-11-8(Hazardous Substances Data)

Upstream product

• 2550-26-7 4-Phenyl-2-butanone 
• 1149-23-1 diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 104-94-9 4-methoxy-aniline 
• 459-60-9 1-fluoro-4-methoxybenzene 
• 22374-89-6 (RS)-1-methyl-3-phenylpropylamine 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 143367-82-2 1-(4-methoxyphenyl)-2-methyl-4-phenyl-1-azabuta-1,3-diene 
• 16520-62-0 4-Phenyl-1-butyne 
• 1311486-17-5 C₁₇H₁₉NO 
• 768-56-9 4-Phenylbut-1-ene 

Downstream Products

• 160191-71-9 (R)-N-(4-methoxyphenyl)-α-methylbenzenepropanamine 
• 73839-93-7 1-methyl-3-phenylpropylamine hydrochloride 
• 22374-89-6 (RS)-1-methyl-3-phenylpropylamine 

Relevant articles and documents

Construction of α-Alkylated Amines by Iridium Complex-Catalyzed One-Step Transfer Hydrogenation of C=C and C=N Bonds

Hydrogenation of C=C bond and reductive amination are important transformations utilized in chemistry. An environmentally friendly, efficient, and facile one-pot transfer hydrogenation of C=C bond of enones and reductive amination of C=N bond of imines are reported using iridium complex as catalysts and formic acid as hydrogen source in aqueous medium. In this catalytic system, a wide range of α-alkylated amines were obtained in excellent yields by one-pot transfer hydrogenation of C=C bond and reductive amination. The practical application of this protocol is characterized by gram-scale transformation.

Amines based on electron-rich fluoroaromatic hydrocarbons, and preparation method of amines

The invention provides amines based on electron-rich fluoroaromatic hydrocarbons, and a preparation method of the amines. The structure of the amines is as shown in a formula I. The invention also provides the preparation method of the amines based on the

Reductive amination catalyzed by iridium complexes using carbon monoxide as a reducing agent

Development of novel, sustainable catalytic methodologies to provide access to amines represents a goal of fundamental importance. Herein we describe a systematic study for the construction of a variety of amines catalyzed by a well-defined homogeneous ir