119707-15-2

Basic information

• Product Name: N-methyl-2-nitro-N-(2-nitrophenyl)aniline
• Synonyms: N-methyl-2-nitro-N-(2-nitrophenyl)aniline
• CAS NO: 119707-15-2
• Molecular Weight: 273.248
• Mol File: 119707-15-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-methyl-2-nitro-N-(2-nitrophenyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyl-2-nitro-N-(2-nitrophenyl)aniline(119707-15-2)
• EPA Substance Registry System: N-methyl-2-nitro-N-(2-nitrophenyl)aniline(119707-15-2)

Safety Data

• Hazardous Substances Data: 119707-15-2(Hazardous Substances Data)

Upstream product

• 18264-71-6 bis(2-nitrophenyl)amine 
• 612-28-2 2-nitro-N-methylaniline 
• 1493-27-2 ortho-nitrofluorobenzene 
• 74-88-4 methyl iodide 
• 88-74-4 2-nitro-aniline 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 93003-41-9 2-methylamino-2'-nitrodiphenylamino 
• 91958-96-2 N-(2-aminophenyl)-N-methylbenzene-1,2-diamine 
• 93003-40-8 N-methyl-N-(2-nitro-phenyl)-o-phenylenediamine 

Relevant articles and documents

Rhodium Complexes Bearing PAlP Pincer Ligands

We report rhodium complexes bearing PAlP pincer ligands with an X-type aluminyl moiety. IR spectroscopy and single-crystal X-ray diffraction analysis of a carbonyl complex exhibit the considerable σ-donating ability of the aluminyl ligand, whose Lewis acidity is confirmed through coordination of pyridine to the aluminum center. The X-type PAlP-Rh complexes catalyze C2-selective monoalkylation of pyridine with alkenes.

The Reduction of Some 2,2'-Dinitrodiaryl Compounds and Related Compounds by Thiourea S,S-Dioxide (Formamidinesulfinic Acid)

The reaction of thiourea S,S-dioxide (formamidinesulfinic acid) in ethanolic alkali with 2,2'-dinitrobiphenyl and several related dinitro compounds possessing an-X-bridge (where X = NH, NMe, O and S), located at the 1,1'-positions, has been investigated.With 2,2'-dinitrobiphenyl (which gives good yields of benzocinnoline and its oxides) and, to a minor extent, with 2,2'-dinitrodiphenylamine, an intramolecular reaction occured to give heterocyclic products; with each of the other dinitro compounds, the only product obtained was formed as the result of a Smiles rearrangement.