5676-82-4

Basic information

• Product Name: N-[(E)-(3-nitrophenyl)methylidene]aniline
• Synonyms: benzenamine, N-[(1E)-(3-nitrophenyl)methylene]-; N-[(E)-(3-Nitrophenyl)methylene]aniline
• CAS NO: 5676-82-4
• Molecular Formula: C₁₃H₁₀N₂O₂
• Molecular Weight: 226.2307
• Mol File: 5676-82-4.mol
• Article Data: 32

Chemical Properties

• Boiling Point: 375.8°C at 760 mmHg
• Flash Point: 181.1°C
• Density: 1.16g/cm³
• Vapor Pressure: 1.64E-05mmHg at 25°C
• Refractive Index: 1.593
• CAS DataBase Reference: N-[(E)-(3-nitrophenyl)methylidene]aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(E)-(3-nitrophenyl)methylidene]aniline(5676-82-4)
• EPA Substance Registry System: N-[(E)-(3-nitrophenyl)methylidene]aniline(5676-82-4)

Safety Data

• Hazardous Substances Data: 5676-82-4(Hazardous Substances Data)

Upstream product

• 99-61-6 3-nitro-benzaldehyde 
• 62-53-3 aniline 
• 135-19-3 β-naphthol 
• 619-25-0 3-Nitrobenzyl alcohol 
• 3489-08-5 (m-nitrobenzylidene)-p-bromoaniline 
• 538-51-2 benzylidene phenylamine 
• 71-43-2 benzene 

Downstream Products

• 40252-71-9 benzylidene-(3-nitro-benzylidene)-hydrazine 
• 17064-90-3 2-nitro-N-(3-nitro-benzyliden)-aniline 
• 538-51-2 benzylidene phenylamine 
• 3430-70-4 N-(3-nitrobenzyl)aniline 
• 144174-47-0 2-(3-nitrophenyl)-3-phenylthiazolidin-4-one 
• 70097-12-0 2-(3-nitro-phenyl)-quinoline-4-carboxylic acid 
• 856209-14-8 [3-Nitro-dl-α-(2-oxy-naphthyl-(1))-benzyl]-anilin 
• 105946-52-9 (E)-1-(4-bromophenyl)-2-(3-nitrobenzylidene)hydrazine 
• 17064-97-0 (3-nitro-benzylidene)-(4-nitro-phenyl)-amine 
• 18885-90-0 3-methyl-5-(3-nitro-phenyl)-4-phenyl-4,5-dihydro-[1,2,4]oxadiazole 
• 78993-85-8 5-[1-(3-Nitro-phenyl)-meth-(E)-ylidene]-2,3-diphenyl-3,5-dihydro-imidazol-4-one 
• 79788-49-1 5-[(3-Nitro-phenyl)-phenylamino-methyl]-3-phenyl-2-thioxo-thiazolidin-4-one 
• 33542-71-1 N-(3-Nitro-benzyl)-N-phenyl-formamide 
• 93-98-1 N-phenyl benzoyl amide 

Relevant articles and documents

Carbon monoxide-driven osmium catalyzed reductive amination harvesting WGSR power

Herein, we present the first example of Os-catalyzed efficient reductive amination under water-gas shift reaction conditions. The developed catalytic systems are formedin situin aqueous solutions, employ as small as 0.0625 mol% osmium and are capable of delivering reductive amination products for a broad range of aliphatic and aromatic carbonyl compounds and amines. The scope of the reaction, active catalytic systems, possible limitations of the method and DFT-supported mechanistic considerations are discussed in detail in the manuscript.

Ru Nanoparticles-Loaded Covalent Organic Framework for Solvent-Free One-Pot Tandem Reactions in Air

Condensation of benzene-1,3,5-tricarbohydrazide with benzene-1,4-dicarboxaldehyde generated a new covalent organic framework, COF-ASB (1), in which the organic units are held together via hydrazone linkage to form porous frameworks. COF-ASB (1) is highly crystalline and displays good chemical and thermal stability and is permanently porous. In addition, 1 can be an ideal support to load Ru nanoparticles (Ru NPs) to generate Ru@COF-ASB (2). The obtained composite material is able to highly promote one-pot tandem synthesis of imine products from benzyl alcohols and corresponding amines under solvent-free conditions in air.

Highly efficient one-pot three-component Betti reaction in water using reverse zinc oxide micelles as a recoverable and reusable catalyst

An efficient synthesis of Betti bases via a one-pot three-component reaction of 2-naphthol, substituted aldehydes and anilines in aqueous media is reported. Through screening different catalysts, reverse zinc oxide nanomicelles show good activity and high