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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)-

3,4-Pyridinedicarboxylic acid, 5-bromo-

OC(=O)c1c(Br)cncc1C(=O)O Request for Quotation
Chemical Name: 3,4-Pyridinedicarboxylic acid, 5-bromo-
CAS Number: 90325-36-3
Product Number: AG006RQH(AGN-PC-03G23W)
Synonyms:
MDL No:
Molecular Formula: C7H4BrNO4
Molecular Weight: 246.0150

Identification/Properties

Properties
BP:
518.632°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

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


5-Bromopyridine-3,4-dicarboxylic acid, also known as 5-Bromo-3,4-pyridinedicarboxylic acid, is a versatile compound with a wide range of applications in chemical synthesis. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceuticals. In particular, 5-Bromopyridine-3,4-dicarboxylic acid is commonly used in the synthesis of heterocyclic compounds, which are essential structural units in many biologically active molecules.By incorporating 5-Bromopyridine-3,4-dicarboxylic acid into a synthesis pathway, chemists can introduce a bromine atom and a pyridine ring into the target molecule, thereby diversifying its chemical properties and functionality. This compound's unique structure allows for the formation of complex structures with specific pharmacological or biological activities. Additionally, the presence of carboxylic acid groups in 5-Bromopyridine-3,4-dicarboxylic acid enables further derivatization and functionalization, enhancing the compound's utility in synthetic chemistry.Overall, the strategic use of 5-Bromopyridine-3,4-dicarboxylic acid in chemical synthesis enables researchers to access a wide array of novel compounds with tailored properties for various applications in drug discovery, materials science, and other fields of organic chemistry.