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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)-

3-Carboxy-5-fluoropyridine-4-boronic acid

OB(c1c(F)cncc1C(=O)O)O Request for Quotation
Chemical Name: 3-Carboxy-5-fluoropyridine-4-boronic acid
CAS Number: 1072952-47-6
Product Number: AG007WI6(AGN-PC-078JO8)
Synonyms:
MDL No:
Molecular Formula: C6H5BFNO4
Molecular Weight: 184.9176

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Borono-5-fluoronicotinic acid is a valuable building block in chemical synthesis due to its unique properties and versatile reactivity. This compound is commonly used as a boronic acid derivative in organic reactions, particularly in Suzuki-Miyaura cross-coupling reactions. In this process, 4-Borono-5-fluoronicotinic acid serves as a key component in the formation of carbon-carbon bonds, allowing for the synthesis of a wide range of complex organic molecules.Additionally, 4-Borono-5-fluoronicotinic acid can undergo various functional group transformations, making it a versatile intermediate in the preparation of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid moiety enables selective and efficient reactions with various electrophiles, providing chemists with a powerful tool for the construction of diverse chemical structures.Furthermore, the presence of the fluorine atom in the 5-position of the nicotinic acid scaffold enhances the compound's reactivity and pharmacological properties, making it an attractive target for drug discovery and development. Overall, the strategic incorporation of 4-Borono-5-fluoronicotinic acid in chemical synthesis offers opportunities for the efficient and controlled assembly of complex organic molecules with diverse applications across the field of medicinal chemistry and materials science.