100-15-2 | N-Methyl-4-nitroaniline

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$6.00	$4.00
25g	95%	in stock	$21.00	$15.00
100g	95%	in stock	$31.00	$22.00
500g	95%	in stock	$137.00	$96.00

Description

• Catalog Number: AA00009
• Chemical Name: N-Methyl-4-nitroaniline
• CAS Number: 100-15-2
• Molecular Formula: C7H8N2O2
• Molecular Weight: 152.1506
• MDL Number: MFCD00007305
• SMILES: CNc1ccc(cc1)[N+](=O)[O-]
• NSC Number: 5390

Computed Properties

• Complexity: 136
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2

Upstream Synthesis Route

N-Methyl-4-Nitroaniline, also known as NMNA, plays a crucial role in chemical synthesis as a versatile building block for the creation of various organic compounds. Due to its unique structural properties, NMNA is commonly used in the pharmaceutical and agrochemical industries to synthesize complex molecules and active ingredients. One of the key applications of N-Methyl-4-Nitroaniline is in the production of dyes and pigments. Its ability to undergo nitration and subsequent reduction reactions make it a valuable precursor for a wide range of colorful and vibrant dyes used in textiles, cosmetics, and other commercial products.Furthermore, NMNA is utilized in the synthesis of heterocyclic compounds, which are essential in the development of pharmaceutical drugs and agrochemicals. By integrating NMNA into various reactions, chemists can construct intricate molecular structures that exhibit biological activity or pesticidal properties.Overall, N-Methyl-4-Nitroaniline serves as a fundamental component in organic synthesis, enabling chemists to design and produce a diverse array of functional molecules with applications across industries.

Literature

• N-Methyl-4-nitro-anilinium chloride.

  Acta crystallographica. Section E, Structure reports online 20120601

• Solvation free energies and hydration structure of N-methyl-p-nitroaniline.

  The Journal of chemical physics 20120421

• Methanolysis of thioamide promoted by a simple palladacycle is accelerated by 10(8) over the methoxide-catalyzed reaction.

  Journal of the American Chemical Society 20111221

• Biological transformation pathways of 2,4-dinitro anisole and N-methyl paranitro aniline in anaerobic fluidized-bed bioreactors.

  Chemosphere 20101101

• Analysis of bacterial community diversity in anaerobic fluidized bed bioreactors treating 2,4-dinitroanisole (DNAN) and n-methyl-4-nitroaniline (MNA) using 16S rRNA gene clone libraries.

  Microbes and environments 20090101

• Physicochemical properties of an insensitive munitions compound, N-methyl-4-nitroaniline (MNA).

  Journal of hazardous materials 20080630

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

• Photoinduced demethylation of 4-nitro-N,N-dimethylaniline.

  Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20020401