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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)-

2,6-Naphthyridin-1-amine

Nc1nccc2c1ccnc2 Request for Quotation
Chemical Name: 2,6-Naphthyridin-1-amine
CAS Number: 80935-81-5
Product Number: AG008LHG(AGN-PC-00JXL9)
Synonyms:
MDL No:
Molecular Formula: C8H7N3
Molecular Weight: 145.1613

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2,6-Naphthyridin-1-amine is a versatile building block commonly used in chemical synthesis. Its unique chemical structure and reactivity make it a valuable tool for creating a wide range of organic compounds. In chemical synthesis, 2,6-Naphthyridin-1-amine can be utilized as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. It serves as a precursor in the synthesis of various heterocyclic compounds, which are essential in drug discovery and development. Additionally, 2,6-Naphthyridin-1-amine can be employed in the construction of complex molecules with specific functionalities, such as fluorescent dyes, materials for electronic applications, and biologically active compounds. Its presence in the synthesis pathway can help introduce nitrogen-containing groups or facilitate cross-coupling reactions to form carbon-carbon bonds.Overall, the use of 2,6-Naphthyridin-1-amine in chemical synthesis enables chemists to access diverse chemical space and design novel molecules with tailored properties and applications.