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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)-

4-Pyridinecarboxylic acid, 2-nitro-

[O-][N+](=O)c1nccc(c1)C(=O)O Request for Quotation
Chemical Name: 4-Pyridinecarboxylic acid, 2-nitro-
CAS Number: 33225-74-0
Product Number: AG003633(AGN-PC-0KKP3W)
Synonyms:
MDL No:
Molecular Formula: C6H4N2O4
Molecular Weight: 168.1070

Identification/Properties

Properties
MP:
174 - 175 °C
BP:
510.174 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
168.108g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
168.017g/mol
Monoisotopic Mass:
168.017g/mol
Topological Polar Surface Area:
96A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
200
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


2-Nitropyridine-4-carboxylic acid is a versatile compound commonly used in chemical synthesis. Its primary application lies in its ability to serve as a precursor in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound is particularly valuable in the pharmaceutical industry, where it is employed as a key building block for the production of a range of bioactive molecules.2-Nitropyridine-4-carboxylic acid is known for its reactivity and compatibility with a variety of other chemical reagents, making it a valuable tool for chemists in the design and development of new compounds. Its unique structure enables it to participate in a wide array of organic reactions, facilitating the creation of complex molecular structures efficiently.Overall, 2-Nitropyridine-4-carboxylic acid plays a crucial role in advancing chemical synthesis by enabling the creation of sophisticated compounds with diverse applications in the fields of medicine, agriculture, and materials science.