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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)-

8-bromo-2-oxo-1H-quinoline-4-carboxylic acid

OC(=O)c1cc(=O)[nH]c2c1cccc2Br Request for Quotation
Chemical Name: 8-bromo-2-oxo-1H-quinoline-4-carboxylic acid
CAS Number: 1248595-74-5
Product Number: AG000MTI(AGN-PC-0ECLOZ)
Synonyms:
MDL No:
Molecular Formula: C10H6BrNO3
Molecular Weight: 268.0635

Identification/Properties

Computed Properties
Molecular Weight:
268.066g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
266.953g/mol
Monoisotopic Mass:
266.953g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
340
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:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


8-Bromo-2-oxo-1,2-dihydroquinoline-4-carboxylic acid is a versatile compound widely used in chemical synthesis due to its unique structural properties and reactivity. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, 8-Bromo-2-oxo-1,2-dihydroquinoline-4-carboxylic acid can undergo various functional group transformations, such as substitution reactions, condensation reactions, and cyclization reactions, to yield a diverse range of molecular structures with specific properties.In medicinal chemistry, this compound is commonly employed for the synthesis of novel drug candidates, particularly in the development of antibacterial and antifungal agents. Its quinoline ring scaffold is known for its pharmacological activities, making it a valuable intermediate in drug discovery research. Furthermore, 8-Bromo-2-oxo-1,2-dihydroquinoline-4-carboxylic acid can be modified through medicinal chemistry techniques to enhance its biological potency, selectivity, and pharmacokinetic properties.Additionally, in the field of material science, this compound can be utilized for the synthesis of functionalized polymers, dyes, and fluorescent probes. Its structural motifs can impart specific properties to these materials, making them suitable for various applications, such as bioimaging, sensors, and optoelectronic devices.Overall, the application of 8-Bromo-2-oxo-1,2-dihydroquinoline-4-carboxylic acid in chemical synthesis provides researchers and chemists with a valuable tool for designing and synthesizing advanced molecular structures with diverse functionalities and applications.