1122-61-8 | 4-Nitropyridine

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$10.00	$7.00
250mg	98%	in stock	$16.00	$12.00
1g	98%	in stock	$49.00	$35.00
2.5g	98%	in stock	$55.00	$39.00
5g	98%	in stock	$89.00	$63.00
10g	98%	in stock	$156.00	$110.00

Description

• Catalog Number: AD41667
• Chemical Name: 4-Nitropyridine
• CAS Number: 1122-61-8
• Molecular Formula: C5H4N2O2
• Molecular Weight: 124.0975
• MDL Number: MFCD29043365
• SMILES: [O-][N+](=O)c1ccncc1
• NSC Number: 30350

Computed Properties

• Complexity: 104
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 3
• XLogP3: 0.3

Upstream Synthesis Route

4-Nitropyridine is a versatile chemical compound commonly utilized in chemical synthesis for its valuable properties and applications. With its nitro group located on the pyridine ring, this compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. In organic synthesis, 4-Nitropyridine is frequently employed as a precursor in the formation of substituted pyridines and heterocyclic compounds. Additionally, it can serve as a valuable intermediate in the synthesis of complex molecules due to its reactivity and compatibility with a range of functional groups. Its versatility and wide range of applications make 4-Nitropyridine an essential tool for chemists working in the field of chemical synthesis.

Literature

• π Back-bonding of iron(II) complexes supported by tris(pyrid-2-ylmethyl)amine and its nitro-substituted derivatives.

  The journal of physical chemistry. A 20111124

• A characterization study on 2,6-dimethyl-4-nitropyridine N-oxide by density functional theory calculations.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20111015

• Systematic coordination chemistry and cytotoxicity of copper(II) complexes with methyl substituted 4-nitropyridine N-oxides.

  Journal of inorganic biochemistry 20110801

• Coordination-induced spin crossover (CISCO) through axial bonding of substituted pyridines to nickel-porphyrins: sigma-donor versus pi-acceptor effects.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20100903

• Mononuclear copper(II) nitrato complexes with methyl-substituted 4-nitropyridine N-oxide. Physicochemical and cytotoxic characteristics.

  Journal of inorganic biochemistry 20100201

• DNA double-strand break repair in parental chromatin of mouse zygotes, the first cell cycle as an origin of de novo mutation.

  Human molecular genetics 20080701

• Chemopreventive effect of fermented brown rice and rice bran on 4-nitroquinoline 1-oxide-induced oral carcinogenesis in rats.

  Oncology reports 20070401

• Well-known quorum sensing inhibitors do not affect bacterial quorum sensing-regulated bean sprout spoilage.

  Journal of applied microbiology 20070301

• Multinuclear 1H, 13C and 15N NMR study of some substituted 2-amino-4-nitropyridines and their N-oxides.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20020501