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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, (3-fluoro-4-methoxyphenyl)-

COc1ccc(cc1F)B(O)O Request for Quotation
Chemical Name: Boronic acid, (3-fluoro-4-methoxyphenyl)-
CAS Number: 149507-26-6
Product Number: AG001LSD(AGN-PC-0KL1I6)
Synonyms:
MDL No:
Molecular Formula: C7H8BFO3
Molecular Weight: 169.9460

Identification/Properties

Properties
MP:
206-211 °C(lit.)
BP:
318.1 °C at 760 mmHg
Storage:
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Fluoro-4-methoxybenzeneboronic acid is a versatile chemical compound widely used in organic synthesis. Its unique structure and properties make it a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. In chemical synthesis, 3-Fluoro-4-methoxybenzeneboronic acid plays a crucial role as a key intermediate in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool in modern organic chemistry for the formation of carbon-carbon bonds. By using 3-Fluoro-4-methoxybenzeneboronic acid as a reactant in this reaction, chemists can efficiently construct complex molecular structures with high precision.Furthermore, this compound can also be utilized in the synthesis of fluorinated aromatic compounds, which are important in the development of new pharmaceuticals and materials. The fluoro and methoxy substituents on the benzene ring offer unique reactivity and selectivity, enabling the synthesis of diverse derivatives with specific functional groups.Overall, the application of 3-Fluoro-4-methoxybenzeneboronic acid in chemical synthesis showcases its significance as a versatile building block for the creation of valuable compounds with potential applications in various fields of chemistry.