486-74-8 | Quinoline-4-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$16.00	$11.00
5g	98%	in stock	$47.00	$33.00
25g	98%	in stock	$198.00	$139.00
100g	98%	in stock	$713.00	$499.00

Description

• Catalog Number: AG24928
• Chemical Name: Quinoline-4-carboxylic acid
• CAS Number: 486-74-8
• Molecular Formula: C10H7NO2
• Molecular Weight: 173.1681
• MDL Number: MFCD00006782
• SMILES: OC(=O)c1ccnc2c1cccc2
• NSC Number: 13138

Computed Properties

• Complexity: 205
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 0.5

Literature

• A simple and convenient copper-catalyzed tandem synthesis of quinoline-2-carboxylates at room temperature.

  The Journal of organic chemistry 20090807

• catena-Poly[zinc(II)-μ-aqua-κO:O-bis-(μ-quinoline-4-carboxyl-ato-κO:O')].

  Acta crystallographica. Section E, Structure reports online 20090801

• Synthesis and biological evaluation of new 4-carboxyl quinoline derivatives as cyclooxygenase-2 inhibitors.

  Bioorganic & medicinal chemistry 20090715

• Synthesis, characterization and crystal structure of novel mononuclear peroxotungsten(VI) complexes. Insulinomimetic activity of W(VI) and Nb(V) peroxo complexes.

  Journal of inorganic biochemistry 20090501

• Tetra-aqua-hexa-kis(μ(2)-quinoline-4-carboxyl-ato)diyttrium(III) dihydrate.

  Acta crystallographica. Section E, Structure reports online 20081201

• Synthesis, antimycobacterial activities and phototoxic evaluation of 5H-thiazolo[3,2-a]quinoline-4-carboxylic acid derivatives.

  Medicinal chemistry (Shariqah (United Arab Emirates)) 20080901

• Tetra-aqua-bis(2-oxo-1,2-dihydro-quinoline-4-carboxyl-ato-κO)nickel(II).

  Acta crystallographica. Section E, Structure reports online 20080201

• Synthesis, structures, and magnetic properties of the copper(II), cobalt(II), and manganese(II) complexes with 9-acridinecarboxylate and 4-quinolinecarboxylate ligands.

  Inorganic chemistry 20051226

• Rapid synthesis of quinoline-4-carboxylic acid derivatives from arylimines and 2-substituted acrylates or acrylamides under indium(III) chloride and microwave activations. Scope and limitations of the reaction.

  Organic & biomolecular chemistry 20051021

• Synthesis and antimycobacterial activities of ring-substituted quinolinecarboxylic acid/ester analogues. Part 1.

  Bioorganic & medicinal chemistry 20040801

• [Experience in the use of chemical compounds for the primary identification and differentiation of enteroviruses].

  Klinicheskaia laboratornaia diagnostika 20030201

• Selection of relevant non-target herbivores for monitoring the environmental effects of Bt maize pollen.

  Environmental biosafety research 20030101

• Unsymmetrical dirhenium complexes that contain [Re(2)](6+) and [Re(2)](5+) cores complexed by tridentate ligands with P(2)O and P(2)N donor sets.

  Inorganic chemistry 20020128

• Recombinant expression of N-terminal truncated mutants of the membrane bound mouse, rat and human flavoenzyme dihydroorotate dehydrogenase. A versatile tool to rate inhibitor effects?

  European journal of biochemistry 20010301

• Species-related inhibition of human and rat dihydroorotate dehydrogenase by immunosuppressive isoxazol and cinchoninic acid derivatives.

  Biochemical pharmacology 19981101