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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)-

(3-bromo-2-chloropyridin-4-yl)boronic acid

OB(c1ccnc(c1Br)Cl)O Request for Quotation
Chemical Name: (3-bromo-2-chloropyridin-4-yl)boronic acid
CAS Number: 1072944-16-1
Product Number: AG008R9X(AGN-PC-0713D6)
Synonyms:
MDL No:
Molecular Formula: C5H4BBrClNO2
Molecular Weight: 236.2588

Identification/Properties

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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (3-Bromo-2-chloropyridin-4-yl)boronic acid is a versatile compound widely used in organic synthesis. It serves as a valuable building block in the development of various pharmaceuticals, agrochemicals, and materials due to its unique reactivity and functional group compatibility. This boronic acid derivative acts as a key reagent in Suzuki-Miyaura cross-coupling reactions, allowing for the efficient formation of carbon-carbon bonds under mild conditions. Its incorporation into organic molecules can lead to the modification of both electronic and steric properties, enabling the fine-tuning of chemical structures for specific applications. Moreover, this compound has found utility in the synthesis of heterocyclic compounds, natural product derivatives, and molecular probes, highlighting its significance in modern organic chemistry.