119-32-4 | 4-Methyl-3-nitroaniline

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$14.00	$10.00
25g	97%	in stock	$40.00	$28.00
100g	97%	in stock	$105.00	$74.00
250g	97%	in stock	$189.00	$132.00

Description

• Catalog Number: AD75017
• Chemical Name: 4-Methyl-3-nitroaniline
• CAS Number: 119-32-4
• Molecular Formula: C7H8N2O2
• Molecular Weight: 152.1506
• MDL Number: MFCD00007910
• SMILES: Nc1ccc(c(c1)[N+](=O)[O-])C
• NSC Number: 7731

Computed Properties

• Complexity: 155
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• XLogP3: 1.7

Upstream Synthesis Route

4-Methyl-3-nitroaniline is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. One of its key applications is as a building block in the production of organic dyes and pigments. This compound serves as a precursor in the synthesis of various colorants used in industries such as textiles, plastics, and printing.Additionally, 4-Methyl-3-nitroaniline plays a crucial role in the manufacturing of pharmaceutical intermediates. Its chemical structure allows for functional group transformations, making it an important starting material for the synthesis of diverse pharmacologically active compounds. This compound's presence in the pharmaceutical industry highlights its significance in drug development and research.In the field of materials science, 4-Methyl-3-nitroaniline is utilized in the synthesis of polymer additives and specialty chemicals. Its reactivity allows for the modification of polymer properties, such as thermal stability, mechanical strength, and chemical resistance. By incorporating this compound into polymer formulations, researchers can tailor material characteristics to meet specific application requirements.Moreover, 4-Methyl-3-nitroaniline is employed in academic research as a model compound for studying organic reactions and mechanisms. The versatile nature of this molecule enables chemists to investigate reaction pathways, functional group transformations, and reactivity trends, contributing to the advancement of organic chemistry knowledge.Overall, the varied applications of 4-Methyl-3-nitroaniline in chemical synthesis underscore its importance as a building block with widespread utility across multiple industries.

Literature

• Bioremediation of 2,4-dinitrotoluene (2,4-DNT) in immobilized micro-organism biological filter.

  Journal of applied microbiology 20110601

• Application of Box-Wilson experimental design method for 2,4-dinitrotoluene treatment in a sequential anaerobic migrating blanket reactor (AMBR)/aerobic completely stirred tank reactor (CSTR) system.

  Journal of hazardous materials 20110315

• Analysis of common and specific mechanisms of liver function affected by nitrotoluene compounds.

  PloS one 20110101

• 5-Diethyl-amino-2-[(E)-(4-methyl-3-nitro-phenyl)-imino-meth-yl]phenol: a redetermination.

  Acta crystallographica. Section E, Structure reports online 20090201

• Toxicological characterization of 2,4,6-trinitrotoluene, its transformation products, and two nitramine explosives.

  Environmental toxicology and chemistry 20070601

• Oxidation of aminonitrotoluenes by 2,4-DNT dioxygenase of Burkholderia sp. strain DNT.

  Biotechnology and bioengineering 20060205

• Graphite-mediated reduction of 2,4-dinitrotoluene with elemental iron.

  Environmental science & technology 20020515

• Surfactant-assisted UV-photolysis of nitroarenes.

  Chemosphere 20020101

• Hydrogen bonding in C-methylated nitroanilines: a room-temperature monoclinic polymorph of 4-methyl-3-nitroaniline with Z' = 2.

  Acta crystallographica. Section C, Crystal structure communications 20011001

• Reduction and Acetylation of 2,4-Dinitrotoluene by a Pseudomonas aeruginosa Strain.

  Applied and environmental microbiology 19960701