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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)-

4-oxo-1H-quinoline-7-carboxylic acid

OC(=O)c1ccc2c(c1)[nH]ccc2=O Request for Quotation
Chemical Name: 4-oxo-1H-quinoline-7-carboxylic acid
CAS Number: 948573-55-5
Product Number: AG0067BD(AGN-PC-05VCE0)
Synonyms:
MDL No:
Molecular Formula: C10H7NO3
Molecular Weight: 189.1675

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
189.17g/mol
XLogP3:
0.1
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:
66.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
298
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of 4-Oxo-1,4-dihydroquinoline-7-carboxylic acid in chemical synthesis lies primarily in its role as a versatile building block for the preparation of various heterocyclic compounds. As a key intermediate, this compound serves as a valuable precursor in the synthesis of structurally diverse molecules with pharmaceutical, agrochemical, and material science applications. By undergoing a series of selective chemical transformations, including cyclization reactions, functional group manipulations, and coupling reactions, 4-Oxo-1,4-dihydroquinoline-7-carboxylic acid can be strategically utilized to access a wide range of complex organic molecules. Its versatility and reactivity make it a crucial component in the synthesis of biologically active compounds and novel materials with tailored properties.