56042-31-0

Basic information

• Product Name: N-Methyl-2,4,6-trinitro-N-phenyl-benzenamine
• CAS NO: 56042-31-0
• Molecular Formula: C₁₃H₁₀N₄O₆
• Molecular Weight: 0
• Mol File: 56042-31-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-Methyl-2,4,6-trinitro-N-phenyl-benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-Methyl-2,4,6-trinitro-N-phenyl-benzenamine(56042-31-0)
• EPA Substance Registry System: N-Methyl-2,4,6-trinitro-N-phenyl-benzenamine(56042-31-0)

Safety Data

• Hazardous Substances Data: 56042-31-0(Hazardous Substances Data)

Upstream product

• 6973-40-6 2,4,6-trinitrophenyl phenyl ether 
• 100-61-8 N-methylaniline 
• 5950-87-8 2,4-dinitrophenyl 2,4,6-trinitrophenyl ether 
• 10242-30-5 2-nitrophenyl 2,4,6-trinitrophenyl ether 
• 103612-93-7 2,6-dinitrophenyl 2,4,6-trinitrophenyl ether 
• 88-88-0 2,4,6-trinitrochlorobenzene 
• 10242-31-6 1-(4-nitrophenoxy)-2,4,6-trinitrobenzene 

Downstream Products

• 62902-37-8 2,4-dibromo-6-chloro-N-methyl-2',4',6'-trinitrodiphenylamine 
• 62902-36-7 2,4,6-trichloro-N-methyl-2',4',6'-trinitrodiphenylamine 

Relevant articles and documents

Anilinolysis of nitro-substituted diphenyl ethers in acetonitrile: the effect of some ortho-substituents on the mechanism of SNAr reactions

Rate data are reported for the reactions of a series of X-phenyl 2,4,6-trinitrophenyl ethers 1a-e [X = H, 4-NO2,2-NO2, 2,4-(NO2)2, or 2,6-(NO2)2] with substituted anilines 2a-e [Y = H, 2-CH

Steric and electronic effects on the mechanism of nucleophilic substitution (SnAr) reactions of some phenyl 2,4,6-trinitrophenyl ethers with aniline and N-methylaniline in acetonitrile and in dimethyl sulfoxide

Rate data are reported for the reactions of a series of 3′- and 4′-substituted phenyl 2,4,6-trinitrophenyl ethers, 4, with aniline in acetonitrile, leading to 2,4,6-trinitrodiphenylamine. The main reaction flux occurs through a base catalysed pathway invo

Rodenticidal use of diphenylamines

A group of diphenylamines, having trinitro substitution or dinitro-trifluoromethyl substitution on one ring and from 1 to 5 substituents of a defined class, particularly halogen atoms, on the other ring, are useful rodenticides.