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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)-

3-Quinolinecarboxylic acid, 6-bromo-4-hydroxy-

Brc1ccc2c(c1)c(O)c(cn2)C(=O)O Request for Quotation
Chemical Name: 3-Quinolinecarboxylic acid, 6-bromo-4-hydroxy-
CAS Number: 98948-95-9
Product Number: AG003N4E(AGN-PC-0OP10D)
Synonyms:
MDL No:
Molecular Formula: C10H6BrNO3
Molecular Weight: 268.0635

Identification/Properties

Properties
BP:
412.069 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
268.066g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-4-hydroxyquinoline-3-carboxylic acid is a key compound widely utilized in chemical synthesis processes. This versatile building block is commonly employed in the pharmaceutical industry for the development of various advanced drug molecules. Its unique structure and functional groups make it a valuable intermediate in synthesizing biologically active compounds. Furthermore, it serves as a crucial precursor in the production of complex organic molecules with diverse applications in medicinal chemistry and drug discovery research. Due to its high reactivity and compatibility with different reaction conditions, 6-Bromo-4-hydroxyquinoline-3-carboxylic acid is an essential component in the modern synthetic chemist's toolkit.