Home Carboxys Quinoline-4-carboxylic acid

Quinoline-4-carboxylic acid

CAS No.:
486-74-8
Catalog Number:
AG00DECO
Molecular Formula:
C10H7NO2
Molecular Weight:
173.1681
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$25
- +
5g
98%
In Stock USA
United States
$88
- +
10g
98%
In Stock USA
United States
$157
- +
25g
98%
In Stock USA
United States
$263
- +
100g
98%
In Stock USA
United States
$1019
- +
Product Description
Catalog Number:
AG00DECO
Chemical Name:
Quinoline-4-carboxylic acid
CAS Number:
486-74-8
Molecular Formula:
C10H7NO2
Molecular Weight:
173.1681
MDL Number:
MFCD00006782
IUPAC Name:
quinoline-4-carboxylic acid
InChI:
InChI=1S/C10H7NO2/c12-10(13)8-5-6-11-9-4-2-1-3-7(8)9/h1-6H,(H,12,13)
InChI Key:
VQMSRUREDGBWKT-UHFFFAOYSA-N
SMILES:
OC(=O)c1ccnc2c1cccc2
EC Number:
207-640-1
NSC Number:
13138
Properties
Complexity:
205  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
173.048g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
173.171g/mol
Monoisotopic Mass:
173.048g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
50.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5  
Literature
Title Journal
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
Properties