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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)-

5-bromo-3-nitropyridine-2-carboxylic acid

[O-][N+](=O)c1cc(Br)cnc1C(=O)O Request for Quotation
Chemical Name: 5-bromo-3-nitropyridine-2-carboxylic acid
CAS Number: 954240-89-2
Product Number: AG0060AB(AGN-PC-07HB3W)
Synonyms:
MDL No: MFCD08061307
Molecular Formula: C6H3BrN2O4
Molecular Weight: 247.0030

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
247.004g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
245.928g/mol
Monoisotopic Mass:
245.928g/mol
Topological Polar Surface Area:
96A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
229
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


5-Bromo-3-nitropicolinic acid is a highly versatile compound widely used in organic synthesis and chemical research. As a potent building block in the field of medicinal chemistry, this compound serves as a key intermediate in the synthesis of various pharmaceuticals and biologically active molecules. It plays a crucial role in the preparation of heterocyclic compounds and is a valuable tool in the development of novel drug candidates targeting specific biological pathways. Additionally, 5-Bromo-3-nitropicolinic acid demonstrates exceptional reactivity in cross-coupling reactions, allowing for the efficient construction of complex molecular structures. Its unique properties make it an essential component in the arsenal of synthetic chemists striving to push the boundaries of chemical innovation.