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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(1H)-Pyridinone, 4-amino-5-nitro-

[O-][N+](=O)c1cnc(cc1N)O Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 4-amino-5-nitro-
CAS Number: 99479-77-3
Product Number: AG005SB0(AGN-PC-00MWJD)
Synonyms:
MDL No:
Molecular Formula: C5H5N3O3
Molecular Weight: 155.1115

Identification/Properties

Properties
BP:
265°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Computed Properties
Molecular Weight:
155.113g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
155.033g/mol
Monoisotopic Mass:
155.033g/mol
Topological Polar Surface Area:
101A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
273
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


4-Amino-5-nitro-2-pyridinol is a versatile compound that finds significant application in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and organic intermediates. Due to its unique structure and reactivity, 4-Amino-5-nitro-2-pyridinol can participate in a range of chemical reactions such as nucleophilic substitutions, condensations, and cyclizations.In chemical synthesis, 4-Amino-5-nitro-2-pyridinol can be used as a key starting material or intermediate to introduce specific functional groups or structural motifs into the desired molecule. Its amino and nitro groups offer opportunities for further derivatization, enabling the synthesis of complex organic compounds with tailored properties.Additionally, the presence of a pyridine ring in 4-Amino-5-nitro-2-pyridinol provides versatility in forming coordination complexes with transition metal catalysts, facilitating various catalytic reactions. This compound's role in chemical synthesis extends to the preparation of dyes, pigments, and other specialty chemicals, highlighting its importance in diverse industrial applications.