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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, (5-fluoro-2-methoxyphenyl)-

COc1ccc(cc1B(O)O)F Request for Quotation
Chemical Name: Boronic acid, (5-fluoro-2-methoxyphenyl)-
CAS Number: 179897-94-0
Product Number: AG0027CR(AGN-PC-0CAGWR)
Synonyms:
MDL No: MFCD01863526
Molecular Formula: C7H8BFO3
Molecular Weight: 169.9460

Identification/Properties

Properties
MP:
144-153 °C(lit.)
BP:
337.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
169.946g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
170.055g/mol
Monoisotopic Mass:
170.055g/mol
Topological Polar Surface Area:
49.7A^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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-2-methoxyphenylboronic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile and valuable building block. This compound is widely utilized in the field of organic chemistry for its ability to participate in various reactions, enabling the construction of complex molecular structures.One key application of $name$ is its use as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronic acid functionality allows for efficient cross-coupling reactions with aryl halides or triflates in the presence of palladium catalysts. This enables the formation of carbon-carbon bonds, facilitating the creation of new carbon frameworks with high efficiency and selectivity.Furthermore, $name$ can also be employed in the preparation of functionalized aromatic compounds, which are essential components in the development of biologically active molecules and materials. Its unique fluorine and methoxy substituents confer specific reactivity and electronic properties to the resulting products, making it a valuable tool for tuning the properties of organic compounds.Overall, the versatility and reactivity of 5-Fluoro-2-methoxyphenylboronic acid make it an indispensable reagent in modern organic synthesis, enabling chemists to access diverse chemical space and drive innovation in drug discovery, materials science, and other research fields.