17064-82-3

Basic information

• Product Name: N-(2-Nitrobenzylidene)-P-toluidine
• Synonyms: N-(2-Nitrobenzylidene)-P-toluidine
• CAS NO: 17064-82-3
• Molecular Formula: C₁₄H₁₂N₂O₂
• Molecular Weight: 240.25728
• Mol File: 17064-82-3.mol
• Article Data: 13

Chemical Properties

• Melting Point: 75 °C
• Boiling Point: 55 °C(Press: 0.1 Torr)
• Appearance: /
• Density: 1.14±0.1 g/cm3(Predicted)
• PKA: 2.88±0.50(Predicted)
• CAS DataBase Reference: N-(2-Nitrobenzylidene)-P-toluidine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-Nitrobenzylidene)-P-toluidine(17064-82-3)
• EPA Substance Registry System: N-(2-Nitrobenzylidene)-P-toluidine(17064-82-3)

Safety Data

• Hazardous Substances Data: 17064-82-3(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 106-49-0 p-toluidine 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 69914-73-4 diethyl {(2-nitrophenyl)[(4-tolyl)amino]methyl}phosphonate 
• 55857-35-7 N-(2-aminobenzylidene)-4-methylaniline 
• 56156-72-0 2-p-tolyl-2H-indazole-3-carbonitrile 
• 109772-95-4 3-cyano-2-(p-tolyl)-2H-indazole 1-oxide 
• 56156-67-3 3-methoxy-4-p-toluidinocinnoline 1-oxide 
• 1204524-90-2 C₃₀H₂₆N₄O₂ 
• 854602-03-2 N-(2-nitrobenzyl)-4-methylaniline 
• 857002-47-2 N-(2-aminobenzyl)-4-methylaniline 
• 3682-73-3 2-(4-methylphenyl)-2H-indazole 
• 55857-35-7 (E)-N-(2-aminobenzylidene)-4-methylaniline 
• 1373546-87-2 2-(4,4,6-trimethyl-1,2,3,4-tetrahydroquinolin-2-yl)aniline 
• 1373545-42-6 N-[2-(4,4,6-Trimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenyl]-methanesulfonamide 
• 1373545-40-4 3-Fluoro-N-[2-(4,4,6-trimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenyl]-benzenesulfonamide 
• 1373545-38-0 N-[2-(4,4,6-Trimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenyl]-benzene sulfonamide 

Relevant articles and documents

Supramolecular Assembly Interceded by C-H···O Hydrogen Bonds and Nitro···π(arene) Interactions of Antibacterial 4-Methyl-(2-nitro benzylidene)aniline using DFT and its Spectral Studies

4-Methyl-(2-nitrobenzylidene)aniline (MNBA) was grown and its structural as well as spectral analyses (FT-IR, FT-Raman, UV and NMR) using experimental and DFT computations were performed to understand its biological applications. Stability of molecule, ch

Facile synthesis of 4-substituted 1,2,4,5-tetrahydro-1,4-benzodiazepin-3-ones by reductive cyclization of 2-chloro-N-(2-nitrobenzyl)acetamides

A facile and efficient method was developed for the synthesis of 1,2,4,5-tetrahydro-1,4-benzodiazepine-3-ones from 2-chloro-N-(2-nitrobenzyl)acetamides through a reductive cyclization using iron-ammonium chloride in ethanol–water in good yields. This method provides a simple approach to these benzodiazepine-3-ones which are of high value in the field of medicinal chemistry research.

A Facile One-Step Synthesis of 2-Arylindazoles via Reductive Cyclization of N-(2-nitroarylidene)amines

A mild and efficient synthesis of 2-arylindazole derivatives via the reductive cyclization of nitro-aryl substrates mediated by a low-valent titanium reagent (TiCl4/Sm/Et3N) has been developed. The attractive features of the current method include an N-N bond formation and the selective reduction of the =C-N bond and nitro group, both of which were easily achieved in one-pot by controlling the pH of the reaction mixture.