15450-76-7 | Quinoline-2,8-diol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$9.00	$6.00
5g	98%	in stock	$9.00	$7.00
10g	98%	in stock	$15.00	$10.00
25g	98%	in stock	$25.00	$17.00
100g	98%	in stock	$87.00	$61.00

Description

• Catalog Number: AB43741
• Chemical Name: Quinoline-2,8-diol
• CAS Number: 15450-76-7
• Molecular Formula: C9H7NO2
• Molecular Weight: 161.1574
• MDL Number: MFCD00216696
• SMILES: Oc1ccc2c(n1)c(O)ccc2
• NSC Number: 108383

Computed Properties

• Complexity: 225
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• XLogP3: 1

Upstream Synthesis Route

2,8-Quinolinediol, also known as quinhydrone, is a versatile compound widely used in chemical synthesis as a redox indicator and a catalyst. It plays a crucial role in various oxidation-reduction reactions due to its ability to undergo reversible redox reactions.In chemical synthesis, 2,8-Quinolinediol is commonly employed as a redox indicator to monitor the progress of reactions. Its characteristic color change from yellow to blue depending on the redox state allows researchers to visually track the reaction kinetics. This makes it an essential tool in the synthesis of organic compounds, enabling precise control over the reaction conditions.Furthermore, 2,8-Quinolinediol serves as a catalyst in numerous organic transformations. Its redox-active properties facilitate electron transfer processes, promoting the formation of desired products in chemical reactions. This catalytic functionality is particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules.Overall, the application of 2,8-Quinolinediol in chemical synthesis showcases its significance as a versatile compound that enhances the efficiency and precision of various reactions, making it a valuable asset in the laboratory setting.

Literature

• Quinoline biodegradation and its nitrogen transformation pathway by a Pseudomonas sp. strain.

  Biodegradation 20100601

• Interaction of 8-hydroxyquinoline with soil environment mediates its ecological function.

  PloS one 20100101

• Aerobic biodegradation characteristics and metabolic products of quinoline by a Pseudomonas strain.

  Bioresource technology 20091101

• [Isolation, identification, and biodegradation characteristics of a quinoline-degrading bacterium].

  Huan jing ke xue= Huanjing kexue 20081201

• A new Hg(2+) -selective fluorescent sensor based on a 1,3-alternate thiacalix[4]arene anchored with four 8-quinolinoloxy groups.

  Inorganic chemistry 20070806

• Configuration-specific synthesis of the facial and meridional isomers of tris(8-hydroxyquinolinate)aluminum (Alq3).

  Inorganic chemistry 20060724

• Antioxidant effects of quinoline alkaloids and 2,4-di-tert-butylphenol isolated from Scolopendra subspinipes.

  Biological & pharmaceutical bulletin 20060401

• Prediction of genotoxicity of chemical compounds by statistical learning methods.

  Chemical research in toxicology 20050601

• 2-Oxoquinoline 8-monooxygenase oxygenase component: active site modulation by Rieske-[2Fe-2S] center oxidation/reduction.

  Structure (London, England : 1993) 20050501

• Antimicrosporidial activity of (fluoro)quinolones in vitro and in vivo.

  Folia parasitologica 20050501

• Conversion of tris(8-quinolinolato-N1, O8) aluminum to 8-hydroxyquinoline and activity in bacterial reverse mutation assays.

  Mutation research 20050404