1. Home
  2. 8-hydroxyquinoline-3-carboxylic acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

8-hydroxyquinoline-3-carboxylic acid

OC(=O)c1cnc2c(c1)cccc2O Request for Quotation
Chemical Name: 8-hydroxyquinoline-3-carboxylic acid
CAS Number: 911109-16-5
Product Number: AG00IGHL(AGN-PC-0BTYQH)
Synonyms:
MDL No:
Molecular Formula: C10H7NO3
Molecular Weight: 189.1675

Identification/Properties

Computed Properties
Molecular Weight:
189.17g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
189.043g/mol
Monoisotopic Mass:
189.043g/mol
Topological Polar Surface Area:
70.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
231
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


8-Hydroxyquinoline-3-carboxylic acid is a versatile compound widely used in chemical synthesis, particularly in the field of coordination chemistry. Its unique structure and properties make it a valuable building block for the preparation of various metal complexes.In chemical synthesis, 8-hydroxyquinoline-3-carboxylic acid serves as a chelating ligand, forming stable complexes with metal ions through coordination bonds. These metal complexes find applications in catalysis, material science, and medicinal chemistry. The ability of 8-hydroxyquinoline-3-carboxylic acid to selectively bind to specific metal ions makes it a valuable tool in designing and synthesizing novel functional materials and pharmaceutical compounds.Furthermore, the presence of both the quinoline and carboxylic acid functional groups in the molecule provides opportunities for derivatization and modification, allowing for the fine-tuning of its properties and reactivity. Overall, the use of 8-hydroxyquinoline-3-carboxylic acid in chemical synthesis opens up a wide range of possibilities for the development of advanced materials and bioactive compounds.