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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-Pyridinecarboxylic acid, 6-amino-5-nitro-

[O-][N+](=O)c1cc(cnc1N)C(=O)O Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 6-amino-5-nitro-
CAS Number: 89488-06-2
Product Number: AG0087RH(AGN-PC-0JO3C0)
Synonyms:
MDL No:
Molecular Formula: C6H5N3O4
Molecular Weight: 183.1216

Identification/Properties

Computed Properties
Molecular Weight:
183.123g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
183.028g/mol
Monoisotopic Mass:
183.028g/mol
Topological Polar Surface Area:
122A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
226
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-H312-H332
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Amino-5-nitronicotinic acid is a versatile chemical compound that finds wide application in the field of chemical synthesis. One of its key uses is as a building block in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds. Due to its unique structure and reactive properties, 6-Amino-5-nitronicotinic acid serves as a valuable precursor in the creation of novel molecules with potential biological activity. In addition, this compound can be utilized in the preparation of diverse heterocyclic compounds through various synthetic pathways, making it a valuable tool in medicinal and materials chemistry. Furthermore, 6-Amino-5-nitronicotinic acid is also employed in the development of ligands for coordination chemistry and catalysis, showcasing its versatility and importance in the realm of chemical synthesis.