613-50-3 | 6-Nitroquinoline

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$10.00	$7.00
5g	98%	in stock	$12.00	$8.00
25g	98%	in stock	$28.00	$19.00

Description

• Catalog Number: AB69991
• Chemical Name: 6-Nitroquinoline
• CAS Number: 613-50-3
• Molecular Formula: C9H6N2O2
• Molecular Weight: 174.15614000000002
• MDL Number: MFCD00006799
• SMILES: [O-][N+](=O)c1ccc2c(c1)cccn2
• NSC Number: 4141

Computed Properties

• Complexity: 202
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• XLogP3: 1.8

Upstream Synthesis Route

6-Nitroquinoline is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various organic molecules. Its unique chemical properties make it a valuable tool for creating a variety of pharmaceuticals, agrochemicals, and materials. In organic synthesis, 6-Nitroquinoline serves as an important intermediate for the synthesis of heterocyclic compounds, which are essential in drug development and other fields. The nitro group on the quinoline ring can undergo various transformation reactions, such as reduction, substitution, and functional group interconversion, allowing for the generation of diverse molecular structures. Additionally, 6-Nitroquinoline can participate in metal-catalyzed reactions, enabling the formation of complex molecules with high efficiency and selectivity. Its versatile reactivity and compatibility with different synthetic methodologies make it a valuable asset in the toolkit of synthetic chemists working in various research areas.

Literature

• Hypoxia-selective, enzymatic conversion of 6-nitroquinoline into a fluorescent helicene: pyrido[3,2-f]quinolino[6,5-c]cinnoline 3-oxide.

  The Journal of organic chemistry 20120406

• Doping control analysis of tricyclic tetrahydroquinoline-derived selective androgen receptor modulators using liquid chromatography/electrospray ionization tandem mass spectrometry.

  Rapid communications in mass spectrometry : RCM 20080801

• [Formations and reactions of aromatic furazan compounds].

  Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20010601