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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-Bromo-3-iodonaphthalene

IC1=CC(Br)=C2C=CC=CC2=C1 Request for Quotation
Chemical Name: 1-Bromo-3-iodonaphthalene
CAS Number: 676267-02-0
Product Number: AG01V5ME()
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


1-Bromo-3-iodonaphthalene is a versatile compound prominently used in chemical synthesis as a key building block. This specialized reagent is particularly valued in the synthesis of various heterocyclic compounds, pharmaceuticals, and advanced materials. Its unique structure, featuring both bromine and iodine functional groups attached to a naphthalene scaffold, offers distinct advantages in synthetic pathways by allowing for selective transformations and controlled reactivity. In organic synthesis, 1-Bromo-3-iodonaphthalene serves as a valuable tool in the creation of complex molecular architectures with precise control over regioselectivity and functional group compatibility. Its strategic role in cross-coupling reactions, halogen exchange processes, and metal-catalyzed transformations highlights its significance in modern chemical research and development. Overall, 1-Bromo-3-iodonaphthalene stands as a crucial reagent that enriches the synthetic chemist's toolbox with enhanced capabilities for designing and constructing intricate organic molecules.