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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)-

Boronic acid, (2-fluoro-5-methylphenyl)-

Cc1ccc(c(c1)B(O)O)F Request for Quotation
Chemical Name: Boronic acid, (2-fluoro-5-methylphenyl)-
CAS Number: 166328-16-1
Product Number: AG001WMP(AGN-PC-0N30YS)
Synonyms:
MDL No: MFCD03428512
Molecular Formula: C7H8BFO2
Molecular Weight: 153.9466

Identification/Properties

Properties
MP:
77-82 °C(lit.)
BP:
291.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
153.947g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
154.06g/mol
Monoisotopic Mass:
154.06g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
132
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


Boronic acid B-(2-fluoro-5-methylphenyl)- is a versatile and valuable reagent in chemical synthesis, especially in organic chemistry. It is widely used in Suzuki-Miyaura coupling reactions, which allow for the formation of carbon-carbon bonds under mild and selective conditions. This particular boronic acid derivative is highly effective in promoting cross-coupling reactions with aryl and heteroaryl halides, enabling the synthesis of a wide range of biaryl compounds. Additionally, it has shown excellent reactivity and compatibility with various functional groups, making it a valuable tool for constructing complex molecular structures in medicinal chemistry, material science, and agrochemical research.