39217-14-6

Basic information

• Product Name: Benzenemethanamine, N-(3,4-dimethoxyphenyl)-
• Synonyms: 3,4-bis(methyloxy)-N-(phenylmethyl)aniline;N-(3,4-dimethoxyphenyl)-N-benzylamine;Benzenemethanamine,N-(3,4-dimethoxyphenyl);4-Benzylamino-veratrol;N-benzyl-4-aminoveratrole
• CAS NO: 39217-14-6
• Molecular Formula: C15H17NO2
• Molecular Weight: 243.305
• Mol File: 39217-14-6.mol
• Article Data: 9

Chemical Properties

• Melting Point: 81-83 °C
• Boiling Point: 170-172 °C(Press: 0.2 Torr)
• Density: 1.118±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzenemethanamine, N-(3,4-dimethoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanamine, N-(3,4-dimethoxyphenyl)-(39217-14-6)
• EPA Substance Registry System: Benzenemethanamine, N-(3,4-dimethoxyphenyl)-(39217-14-6)

Safety Data

• Hazardous Substances Data: 39217-14-6(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 6315-89-5 3,4-dimethoxyaniline 
• 13548-24-8 (3,4-Dimethoxy-phenyl)-[1-phenyl-meth-(E)-ylidene]-amine 
• 100-51-6 benzyl alcohol 

Downstream Products

• 931399-59-6 ethyl 1-benzyl-4-hydroxy-6,7-dimethoxy-2-oxo-1,2-dihydroquinoline-3-carboxylate 
• 1537188-64-9 ethyl 3-(benzyl(3,4-dimethoxyphenyl)amino)-3-oxopropanoate 
• 59632-34-7 4-[(4-phenyl-1-piperazinyl)carbonyl]-9-benzyl-6,7-dimethoxy-1,2,3,4-tetrahydrocarbazole 
• 59632-33-6 9-benzyl-6,7-dimethoxy-1,2,3,4-tetrahydro-carbazole-4-carboxylic acid 
• 148518-76-7 N-benzyl-N-(3,4-dimethoxyphenyl)-α-carbomethoxy-α-diazoacetamide 
• 161885-41-2 N-<3-N-(3,4-dimethoxyphenyl)propylamino>-7,8-dimethoxy-2,3,4,5-tetrahydro-2-oxo-1H-3-benzazepin 

Relevant articles and documents

Nickel?Copper bimetallic mesoporous nanoparticles: As an efficient heterogeneous catalyst for N-alkylation of amines with alcohols

A bimetallic catalyst (Ni/Cu-MCM-41) is prepared via co-condensation method. The latter is characterized by Fourier transform infrared (FT-IR), X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), diffuse reflectance spectroscopy (DRS), and nitrogen adsorption–desorption analysis. Catalytic performance of Ni/Cu-MCM-41 is probed in N-alkylation of amines with alcohols through a hydrogen autotransfer process. Noteworthy, this catalytic system appears very efficient for synthesis of a range of secondary and tertiary amines in good to excellent isolated yields. Moreover, the catalyst is successfully recovered and reused four times without notable decrease in its activity.

N-substituted thiourea or urea derivatives and pharmaceutical composition for use in preventing or treating glutaminyl cyclase activity related diseases containing the same as an active ingredient

The N - substituted thiourea or urea derivative and the pharmaceutical composition for preventing or treating glutaminyl cyclase (QC) activity containing the same as an active ingredient. The phenylthiourea derivative according to the present invention bi

A nanoscale iron catalyst for heterogeneous direct: N - And C -alkylations of anilines and ketones using alcohols under hydrogen autotransfer conditions

Here, we report a commercially available nanoscale Fe catalyst for heterogeneous direct N- and C-alkylation reactions of anilines and methyl ketones with alcohols. A hydrogen autotransfer mechanism has been found to operate in these reactions by deuterium labelling studies. In addition, dehydrogenative quinoline synthesis has been demonstrated from amino benzyl alcohols and acetophenones.