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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)-

5-bromo-1,6-naphthyridine

Brc1nccc2c1cccn2 Request for Quotation
Chemical Name: 5-bromo-1,6-naphthyridine
CAS Number: 68336-81-2
Product Number: AG00646Q(AGN-PC-0NJ1KU)
Synonyms:
MDL No:
Molecular Formula: C8H5BrN2
Molecular Weight: 209.0427

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-1,6-naphthyridine, a heterocyclic compound, finds its primary application in chemical synthesis as a versatile building block in the creation of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure and reactivity, 5-Bromo-1,6-naphthyridine serves as a valuable intermediate in the synthesis of complex organic molecules. It can participate in various reactions such as palladium-catalyzed cross-coupling reactions, nucleophilic aromatic substitutions, and metal-catalyzed transformations. The bromine atom on the naphthyridine ring increases the compound's reactivity and allows for further functionalization, making it a key component in the development of novel compounds with diverse biological activities and industrial applications.