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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)-

4-BroMoMethyl-3-fluoropyridine

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Chemical Name: 4-BroMoMethyl-3-fluoropyridine
CAS Number: 1227602-49-4
Product Number: AG009COY(AGN-PC-0WAKB6)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


4-Bromomethyl-3-fluoropyridine is a valuable chemical intermediate widely used in organic synthesis. One of its key applications is in the synthesis of pharmaceutical compounds, where it serves as a versatile building block for the modification of molecular structures.Due to its unique reactivity, 4-Bromomethyl-3-fluoropyridine can participate in various types of chemical reactions such as nucleophilic substitutions, palladium-catalyzed cross-coupling reactions, and lithiation reactions. This enables the efficient introduction of functional groups or the formation of complex molecular scaffolds, making it an essential tool in medicinal chemistry and drug development.Moreover, the presence of both bromine and fluorine atoms in 4-Bromomethyl-3-fluoropyridine enhances the diversity of synthetic pathways that can be accessed, allowing for the creation of novel molecules with enhanced biological activity or pharmacokinetic properties. Its versatility and utility in chemical synthesis make 4-Bromomethyl-3-fluoropyridine a valuable asset for researchers and chemists seeking to design and produce new pharmaceutical compounds.