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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-bromo-6-fluoro-3-methoxyphenyl)boronic acid

COc1ccc(c(c1Br)B(O)O)F Request for Quotation
Chemical Name: (2-bromo-6-fluoro-3-methoxyphenyl)boronic acid
CAS Number: 957062-89-4
Product Number: AG003BLZ(AGN-PC-00UQV6)
Synonyms:
MDL No:
Molecular Formula: C7H7BBrFO3
Molecular Weight: 248.8421

Identification/Properties

Properties
MP:
130-135℃
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
248.842g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
247.966g/mol
Monoisotopic Mass:
247.966g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
172
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (2-Bromo-6-fluoro-3-methoxyphenyl)boronic acid, a versatile chemical compound, serves as a crucial building block in chemical synthesis due to its unique properties and reactivity. This compound is extensively used in copper-catalyzed coupling reactions to introduce the functional group –BF₂ moiety into various organic molecules.In organic chemistry, it acts as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and organic halides or pseudo-halides. This process allows for the efficient construction of complex organic structures, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and materials science.Furthermore, the (2-Bromo-6-fluoro-3-methoxyphenyl)boronic acid can also be employed in transition metal-catalyzed C-H activation reactions, facilitating the direct functionalization of C-H bonds in aromatic compounds. This approach offers a more sustainable and atom-efficient route to modify organic molecules, reducing the reliance on pre-functionalized starting materials.Overall, the application of (2-Bromo-6-fluoro-3-methoxyphenyl)boronic acid in chemical synthesis showcases its significance as a versatile reagent for constructing complex molecules and advancing the field of organic chemistry.