2-Hydroxy-5-nitronicotinamide|941083-49-4,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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-Hydroxy-5-nitronicotinamide

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Chemical Name:	2-Hydroxy-5-nitronicotinamide
CAS Number:	941083-49-4
Product Number:	AG01DOBV(AGN-PC-0WAIG9)
Synonyms:
MDL No:
Molecular Formula:	C6H5N3O4
Molecular Weight:	183.1216

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Chemical Structure

2-Hydroxy-5-nitronicotinamide, a versatile chemical compound, plays a crucial role in chemical synthesis as a building block in various reactions. Its unique structure and properties make it ideal for use in organic transformations and the creation of complex molecules. As a key intermediate, 2-Hydroxy-5-nitronicotinamide is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Its ability to undergo various functional group conversions enables chemists to efficiently access diverse derivatives with tailored properties for specific applications. Furthermore, the presence of both a hydroxyl and nitro group on the nicotinamide scaffold provides opportunities for selective functionalization and the development of novel chemical entities with enhanced biological activities.