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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)-

2,5-dibromopyridine-4-carboxylic acid

Brc1ncc(c(c1)C(=O)O)Br Request for Quotation
Chemical Name: 2,5-dibromopyridine-4-carboxylic acid
CAS Number: 942473-59-8
Product Number: AG00GUA3(AGN-PC-056MVS)
Synonyms:
MDL No:
Molecular Formula: C6H3Br2NO2
Molecular Weight: 280.9015

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
280.903g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
280.851g/mol
Monoisotopic Mass:
278.853g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
165
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Pyridinecarboxylic acid, 2,5-dibromo- is a versatile compound commonly employed in chemical synthesis. This particular derivative of pyridinecarboxylic acid is valued for its ability to serve as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, 4-Pyridinecarboxylic acid, 2,5-dibromo- is utilized as a crucial intermediate in the preparation of biologically active compounds. Its unique molecular structure, characterized by the presence of bromine atoms at the 2 and 5 positions, enables it to participate in a range of selective and efficient synthetic transformations.The presence of bromine substituents in this compound enhances its reactivity and allows for facile functionalization to introduce diverse chemical functionalities. This makes 4-Pyridinecarboxylic acid, 2,5-dibromo- a valuable tool for introducing specific structural motifs into target molecules during the synthesis of complex organic compounds.Chemists utilize 4-Pyridinecarboxylic acid, 2,5-dibromo- in various chemical reactions such as coupling reactions, halogenation, and Suzuki-Miyaura cross-coupling reactions to construct highly functionalized molecules with precision. Its strategic positioning of bromine atoms within the pyridine ring facilitates regioselective transformations, enabling the synthesis of novel compounds with tailored properties and functionalities.Overall, 4-Pyridinecarboxylic acid, 2,5-dibromo- plays a pivotal role in the realm of chemical synthesis by providing chemists with a versatile and synthetically valuable building block for the construction of diverse molecular architectures with potential applications across multiple scientific disciplines.