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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-Fluoropyridine-2-boronic acid pinacol ester

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Chemical Name: 4-Fluoropyridine-2-boronic acid pinacol ester
CAS Number: 1260152-43-9
Product Number: AG009BZS(AGN-PC-0WAG61)
Synonyms:
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Molecular Formula:
Molecular Weight:

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Chemical Structure


4-Fluoropyridin-2-ylboronic acid pinacol ester plays a crucial role in chemical synthesis as a versatile building block. It serves as a valuable reagent in various cross-coupling reactions, particularly in Suzuki-Miyaura coupling reactions to form carbon-carbon bonds. This compound is highly sought after in organic synthesis for its ability to introduce the 4-fluoropyridin-2-yl moiety efficiently into target molecules. Additionally, its boronic acid functionality enables selective manipulation of aromatic systems, making it a powerful tool for constructing complex molecular structures. In medicinal chemistry, this compound finds application in the synthesis of pharmaceuticals and agrochemicals due to the prevalence of the pyridine scaffold in bioactive compounds.