1,5-Naphthyridin-2(1H)-one, 3-nitro-|64222-33-9,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)-

1,5-Naphthyridin-2(1H)-one, 3-nitro-

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Chemical Name:	1,5-Naphthyridin-2(1H)-one, 3-nitro-
CAS Number:	64222-33-9
Product Number:	AG00EG6I(AGN-PC-0NJJ5K)
Synonyms:
MDL No:
Molecular Formula:	C8H5N3O3
Molecular Weight:	191.1436

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Chemical Structure

3-Nitro-1,5-naphthyridin-2(1H)-one serves as a valuable building block in chemical synthesis due to its versatile reactivity and unique structure. This compound is commonly employed as a precursor in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its nitro group can be easily transformed into different functional groups, such as amino or hydroxyl groups, through reduction or nucleophilic substitution reactions. Additionally, the naphthyridinone scaffold provides a rigid and planar structure that is advantageous for designing molecules with specific biological activities or physical properties. The versatility of 3-Nitro-1,5-naphthyridin-2(1H)-one makes it a valuable intermediate in the production of diverse compounds with potential applications in medicinal chemistry and material science.