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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)-

(6-bromo-5-methylpyridin-3-yl)boronic acid

OB(c1cnc(c(c1)C)Br)O Request for Quotation
Chemical Name: (6-bromo-5-methylpyridin-3-yl)boronic acid
CAS Number: 1003043-34-2
Product Number: AG0001JK(AGN-PC-01LR0I)
Synonyms:
MDL No: MFCD08274468
Molecular Formula: C6H7BBrNO2
Molecular Weight: 215.8403

Identification/Properties

Properties
BP:
378.9°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
215.841g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
214.975g/mol
Monoisotopic Mass:
214.975g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
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


(6-Bromo-5-methylpyridin-3-yl)boronic acid is a versatile compound widely used in chemical synthesis as a valuable building block for creating complex organic molecules. This boronic acid derivative is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a powerful tool in organic synthesis for forming carbon-carbon bonds.In the context of chemical synthesis, this compound serves as a key component for constructing biaryl systems, a common motif found in pharmaceuticals, agrochemicals, and materials science. By participating in C-C bond formation reactions, (6-Bromo-5-methylpyridin-3-yl)boronic acid enables the creation of novel molecular structures with tailored properties and functions.Furthermore, this boronic acid derivative can be utilized in the preparation of ligands for transition metal-catalyzed coupling reactions, offering a route to diverse functionalized organic compounds. Its compatibility with various reaction conditions and substrates makes it a valuable reagent for designing and synthesizing complex molecules in the field of medicinal chemistry, materials science, and chemical biology.Overall, the application of (6-Bromo-5-methylpyridin-3-yl)boronic acid in chemical synthesis highlights its significance as a strategic building block for constructing diverse organic molecules with tailored properties and functionalities.