55578-14-8

Basic information

• Product Name: Benzenemethanamine, N-(1-methylethyl)-N-(phenylmethyl)-
• Synonyms: N,N-dibenzylisoprpopylamine;2-Propanamine,N,N-dibenzyl;dibenzyl-isopropyl-amine;N,N-Dibenzyl-2-propanamine;Dibenzyl-isopropyl-amin;N,N-dibenzylisopropylamine
• CAS NO: 55578-14-8
• Molecular Formula: C17H21N
• Molecular Weight: 239.36
• Mol File: 55578-14-8.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 317.4±11.0 °C(Predicted)
• Density: 0.996±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzenemethanamine, N-(1-methylethyl)-N-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanamine, N-(1-methylethyl)-N-(phenylmethyl)-(55578-14-8)
• EPA Substance Registry System: Benzenemethanamine, N-(1-methylethyl)-N-(phenylmethyl)-(55578-14-8)

Safety Data

• Hazardous Substances Data: 55578-14-8(Hazardous Substances Data)

Upstream product

• 102-97-6 Benzyl-isopropyl-amin 
• 67-64-1 acetone 
• 103-49-1 dibenzylamine 
• 60479-65-4 (S)-2-(N,N-dibenzylamino)-1-propanol 
• 75-31-0 isopropylamine 
• 100-51-6 benzyl alcohol 
• 100-39-0 benzyl bromide 
• 780-25-6 N-benzylidene benzylamine 
• 618-32-6 Benzoyl bromide 
• 5440-69-7 N-isopropylbenzamide 
• 52742-32-2 N,N-dibenzyl-O-benzoylhydroxylamine 
• 625-81-0 diisopropyl zinc 
• 105680-00-0 N-benzyl-N-isopropylbenzamide 

Downstream Products

• 5440-69-7 N-isopropylbenzamide 

Relevant articles and documents

Reductive amination of ketones/aldehydes with amines using BH3N(C2H5)3as a reductant

Herein, we report the first example of efficient reductive amination of ketones/aldehydes with amines using BH3N(C2H5)3 as a catalyst and a reductant under mild conditions, affording various tertiary and secondary amines in excellent yields. A mechanistic study indicates that BH3N(C2H5)3 plays a dual function role of promoting imine and iminium formation and serving as a reductant in reductive amination. This journal is

The synthesis of sterically hindered amines by a direct reductive amination of ketones

An atom-economical methodology for the synthesis of sterically hindered tertiary amines was developed, which is based on complementary Rh- and Ru-catalyzed direct reductive amination of ketones with primary and secondary amines using carbon monoxide as a deoxygenating agent.

N-alkylation of amines by homogeneous ruthenium complexes in the presence of free diphosphines

Chemoselective N-alkylation of amines by ruthenium complexes in the presence of free diphosphine ligands under mild conditions is described. Octyl amine and aniline were chosen as aliphatic and aromatic amines to investigate the effect of different phosphines, reaction times, and temperature on conversion, as well as selectivity towards related secondary and tertiary amines. After optimization of the reaction conditions, this catalytic system was used for N-alkylation of other amines and has shown moderate to very good yields. The reaction products were monitored by GC-MS. The crystal structure of [Ru(NO3)2CO(PPh3)2] with a monodentate and a bidentate nitrate was determined by X-ray crystallographic analysis.