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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)-

1,6-Naphthyridin-2(1H)-one, 1-methyl-

Cn1c(=O)ccc2c1ccnc2 Request for Quotation
Chemical Name: 1,6-Naphthyridin-2(1H)-one, 1-methyl-
CAS Number: 148244-93-3
Product Number: AG001FJE(AGN-PC-02JNRK)
Synonyms:
MDL No:
Molecular Formula: C9H8N2O
Molecular Weight: 160.1726

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Chemical Structure


1-Methyl-1,6-naphthyridin-2(1H)-one, also known as $name$, is a versatile compound commonly used in chemical synthesis. It serves as a key building block for the creation of various organic molecules due to its unique structural properties and reactivity. In the realm of chemical synthesis, $name$ acts as a precursor in the preparation of heterocyclic compounds and pharmaceutical intermediates. Its presence in the synthesis process allows for the formation of diverse carbon-carbon and carbon-nitrogen bonds, essential for the production of complex organic molecules. In addition, the functional groups present in $name$ enable selective derivatization, facilitating the preparation of custom-designed molecules for specific applications in drug discovery, material science, and agrochemicals. The use of 1-Methyl-1,6-naphthyridin-2(1H)-one in chemical synthesis exemplifies its significance as a valuable tool for researchers and chemists striving to develop innovative and impactful compounds.