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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)-

2,4-Quinolinedicarboxylic acid, 6-bromo-

Brc1ccc2c(c1)c(cc(n2)C(=O)O)C(=O)O Request for Quotation
Chemical Name: 2,4-Quinolinedicarboxylic acid, 6-bromo-
CAS Number: 250641-14-6
Product Number: AG002QC0(AGN-PC-0JY20Q)
Synonyms:
MDL No:
Molecular Formula: C11H6BrNO4
Molecular Weight: 296.0736

Identification/Properties

Computed Properties
Molecular Weight:
296.076g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
294.948g/mol
Monoisotopic Mass:
294.948g/mol
Topological Polar Surface Area:
87.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
335
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

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Chemical Structure


6-Bromoquinoline-2,4-dicarboxylic acid is a versatile building block in chemical synthesis, prized for its unique properties and wide range of applications. This compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds.In organic synthesis, 6-Bromoquinoline-2,4-dicarboxylic acid is utilized as a precursor for the preparation of diverse quinoline derivatives. These derivatives are important in medicinal chemistry due to their potent biological activities, such as antimicrobial, anti-inflammatory, and anticancer properties.Furthermore, this compound can be employed as a ligand in coordination chemistry, forming complexes with various metal ions. These complexes exhibit intriguing catalytic properties and are utilized in the synthesis of complex natural products and pharmaceuticals.Overall, 6-Bromoquinoline-2,4-dicarboxylic acid plays a crucial role in the realm of chemical synthesis, enabling the construction of complex molecular structures with diverse functionalities and biological activities.