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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-chloro-2-fluoropyridin-4-yl)boronic acid

OB(c1ccnc(c1Cl)F)O Request for Quotation
Chemical Name: (3-chloro-2-fluoropyridin-4-yl)boronic acid
CAS Number: 1217500-55-4
Product Number: AG0015PD(AGN-PC-0786MI)
Synonyms:
MDL No:
Molecular Formula: C5H4BClFNO2
Molecular Weight: 175.3532

Identification/Properties

Properties
MP:
126-130°C
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
175.35g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
175.001g/mol
Monoisotopic Mass:
175.001g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
140
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (3-Chloro-2-fluoropyridin-4-yl)boronic acid is a versatile and valuable building block in chemical synthesis. This compound is widely utilized in organic chemistry as a key reagent for the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its unique combination of fluorine, chlorine, and boronic acid functional groups make it particularly useful in the development of new chemical entities and drug discovery research. In particular, this compound serves as a crucial intermediate in Suzuki-Miyaura cross-coupling reactions, allowing for the efficient and selective formation of carbon-carbon bonds. The (3-Chloro-2-fluoropyridin-4-yl)boronic acid provides chemists with a powerful tool for the construction of complex molecular structures, enabling the synthesis of diverse chemical compounds with enhanced biological or physical properties.