7119-93-9

Basic information

• Product Name: N-methyl-N-nitroaniline
• CAS NO: 7119-93-9
• Molecular Formula: C₇H₈N₂O₂
• Molecular Weight: 152.1506
• Mol File: 7119-93-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 287.6°C at 760 mmHg
• Flash Point: 127.8°C
• Density: 1.23g/cm³
• Vapor Pressure: 0.00246mmHg at 25°C
• Refractive Index: 1.593
• CAS DataBase Reference: N-methyl-N-nitroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyl-N-nitroaniline(7119-93-9)
• EPA Substance Registry System: N-methyl-N-nitroaniline(7119-93-9)

Safety Data

• Hazardous Substances Data: 7119-93-9(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 645-55-6 N-nitroaniline 
• 77-78-1 dimethyl sulfate 
• 100-61-8 N-methylaniline 
• 6786-32-9 benzoyl nitrate 
• 74-88-4 methyl iodide 
• 60-29-7 diethyl ether 
• 67-56-1 methanol 
• 124-41-4 sodium methylate 
• 58682-35-2 potassium benzene-anti-diazotate 
• 121-69-7 N,N-dimethyl-aniline 

Downstream Products

• 618-40-6 1-Methyl-1-phenylhydrazine 
• 612-28-2 2-nitro-N-methylaniline 
• 479-45-8 tetryl 
• 64-18-6 formic acid 
• 7782-77-6 cis-nitrous acid 
• 62-53-3 aniline 
• 100-61-8 N-methylaniline 
• 614-00-6 N-methyl-N-nitrosoaniline 
• 7664-41-7 ammonia 
• 100-15-2 N-methyl(p-nitroaniline) 
• 16698-03-6 N-nitro-N-methyl-4-nitroaniline 
• 943-41-9 N-methyl-N-nitroso-4-nitroaniline 
• 58538-01-5 N-methyl-N-nitroso-2,4-dinitroaniline 
• 2044-88-4 N-methyl-2,4-dinitroaniline 

Relevant articles and documents

Synthesis method of nitramide

The invention relates to a synthesis method of nitramide. The method comprises the step of enabling an aniline reaction substrate and a nitrating reagent to be subjected to a reaction in a solvent at20-60 DEG C for 2-8 hours to obtain the nitramide, where

AN ALTERNATE METHOD FOR THE SYNTHESIS OF SECONDARY NITRAMINES

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SUBSTITUENT EFFECT TREATMENT OF INTERACTIONS BETWEEN CONTIGUOUS FUNCTIONALITIES. IV. RESTRAINT TO PHENYL-NITROGEN CONJUGATIVE INTERACTION IN N-FUNCTIONALIZED N-METHYLANILINES

13C shifts at the para position in PhN(Me)X for 17 different substituents X serve as monitors for investigating, in correlative analysis, the nature and the extent of interactions occurring between the substituent X and the N-Me cavity.For the majority of substituent, X, partitioning of the nitrogen electron pair between the phenyl and the substituent is partially hampered because of the non-zero twist angle between the planes containing the phenyl ring and the Me-N-X fragment.As a consequence, relative to PhNHX, the interactions between the cavity and the substituents are increased in intensity, especially their mesomeric component, and, at the same time, para-13C shifts are displaced toward lower field.Evidence is also provided that possible H-bonding by the NH cavity of PhNHX with dimethyl sulphoxide does not appreciably influence the substituent electron demand determined previously.