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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)-

[2-fluoro-5-(hydroxymethyl)phenyl]boronic acid

OCc1ccc(c(c1)B(O)O)F Request for Quotation
Chemical Name: [2-fluoro-5-(hydroxymethyl)phenyl]boronic acid
CAS Number: 1072952-25-0
Product Number: AG007WI7(AGN-PC-0786J1)
Synonyms:
MDL No:
Molecular Formula: C7H8BFO3
Molecular Weight: 169.9460

Identification/Properties

Computed Properties
Molecular Weight:
169.946g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
170.055g/mol
Monoisotopic Mass:
170.055g/mol
Topological Polar Surface Area:
60.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
145
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 (2-Fluoro-5-(hydroxymethyl)phenyl)boronic acid is a versatile reagent commonly used in organic synthesis for the preparation of various important molecules. This compound serves as a valuable building block in Suzuki-Miyaura cross-coupling reactions, a widely employed method in modern organic chemistry for the formation of carbon-carbon bonds. The boronic acid functionality enables selective and efficient coupling with aryl halides or pseudohalides, opening up a wide range of synthetic possibilities.Moreover, the hydroxymethyl group in the (2-Fluoro-5-(hydroxymethyl)phenyl)boronic acid provides additional flexibility in functional group transformations, allowing for the introduction of various functional groups through straightforward synthetic manipulations. This versatility makes it a valuable tool for the construction of complex molecules in medicinal chemistry, material science, and agrochemical research.Overall, the (2-Fluoro-5-(hydroxymethyl)phenyl)boronic acid plays a crucial role in enabling efficient and selective chemical synthesis processes, making it an indispensable reagent in modern organic chemistry research and application.