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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)-

(4-bromo-6-chloropyridin-3-yl)boronic acid

OB(c1cnc(cc1Br)Cl)O Request for Quotation
Chemical Name: (4-bromo-6-chloropyridin-3-yl)boronic acid
CAS Number: 957062-85-0
Product Number: AG003BUS(AGN-PC-0713DZ)
Synonyms:
MDL No:
Molecular Formula: C5H4BBrClNO2
Molecular Weight: 236.2588

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
236.256g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
234.921g/mol
Monoisotopic Mass:
234.921g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
140
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:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (4-Bromo-6-chloropyridin-3-yl)boronic acid is a versatile compound commonly used in chemical synthesis as a key building block for the preparation of various pharmaceuticals, agrochemicals, and materials. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, a fundamental transformation in organic chemistry that enables the formation of carbon-carbon bonds. By serving as a coupling partner in this reaction, (4-Bromo-6-chloropyridin-3-yl)boronic acid facilitates the construction of more complex molecular structures with precision and efficiency. Its unique combination of bromine and chlorine substituents on the pyridine ring confers specific reactivity patterns that are exploited by synthetic chemists to access a wide range of functionalized compounds. The use of (4-Bromo-6-chloropyridin-3-yl)boronic acid in chemical synthesis empowers researchers to access diverse chemical space and accelerate the discovery and development of new biologically active molecules and advanced materials.