730-39-2

Basic information

• Product Name: Benzenamine, 4-methyl-N-[(4-nitrophenyl)methylene]-
• CAS NO: 730-39-2
• Molecular Formula: C14H12N2O2
• Molecular Weight: 240.261
• Mol File: 730-39-2.mol
• Article Data: 25

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-methyl-N-[(4-nitrophenyl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-methyl-N-[(4-nitrophenyl)methylene]-(730-39-2)
• EPA Substance Registry System: Benzenamine, 4-methyl-N-[(4-nitrophenyl)methylene]-(730-39-2)

Safety Data

• Hazardous Substances Data: 730-39-2(Hazardous Substances Data)

Upstream product

• 21646-74-2 1-nitro-2-(4-nitrophenyl)-1-ethoxycarbonylethene 
• 106-49-0 p-toluidine 
• 71-43-2 benzene 
• 461670-18-8 ethyl (2RS,3RS)-2-nitro-3-nitro-oxy-3-(4-nitrophenyl)propionate 
• 39203-82-2 N-(4-cyanobenzylidene)-4-methylaniline 
• 25105-94-6 N-(4-nitrophenylmethylidene)-n-butylamine 
• 785-80-8 p-nitrobenzylideneaniline 
• 555-16-8 4-nitrobenzaldehdye 
• 622-58-2 p-Tolylisocyanate 
• 619-73-8 4-nitrobenzyl chloride 

Downstream Products

• 1207463-74-8 1-(4-nitrophenyl)-1-(p-tolylamino)hexan-3-one 
• 38940-30-6 1-(4-nitrophenyl)-1-(p-tolylamino)pentan-3-one 
• 16035-83-9 N-(4-nitro-benzyl)-p-toluidine 
• 25105-94-6 N-(4-nitrophenylmethylidene)-n-butylamine 
• 106-49-0 p-toluidine 
• 785-80-8 p-nitrobenzylideneaniline 

Relevant articles and documents

Synthesis of Green/Blue Light Emitting Quinolines by Aza-D-A Reaction Using InCl3 Catalyst

An efficient InCl3-catalyzed sequential reaction of aromatic amines, aromatic aldehydes and functionalized alkynes leading to the formation of new quinoline derivatives exhibiting significant fluorescence activities is described. The photophysi

Dehydrogenation and α-functionalization of secondary amines by visible-light-mediated catalysis

A visible-light-mediated process for dehydrogenation of amines has been described. The given protocol showed a broad substrate scope, mild reaction conditions and excellent results without the requirement of tedious purification. This process can be applied in one-pot functionalization of secondary amines with various nucleophiles through the cooperation of visible-light and Lewis acid catalysis, leading to the structurally varied essential components of biologically active molecules. In addition, Stern-Volmer studies and quenching experiments revealed the role of a catalyst and led to the proposed mechanism of this transformation.

Dual Heterogeneous Catalyst Pd-Au@Mn(II)-MOF for One-Pot Tandem Synthesis of Imines from Alcohols and Amines

A new Mn(II) metal-organic framework (MOF) 1 was synthesized by the combination of 4,4,4-trifluoro-1-(4-(pyridin-4-yl)phenyl)butane-1,3-dione (L) and Mn(OAc)2 in solution. 1 features a threefold-interpenetrating NbO net containing honeycomb-like channels, in which the opposite Mn(II)···Mn(II) distance is 23.5075(10) ?. Furthermore, 1 can be an ideal platform to support Pd-Au bimetallic alloy nanoparticles to generate a composite catalytic system of Pd-Au@Mn(II)-MOF (2). 2 can be a highly active bifunctional heterogeneous catalyst for the one-pot tandem synthesis of imines from benzyl alcohols and anilines and from benzyl alcohols and benzylamines.