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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)-

(2,5-dibromopyridin-3-yl)boronic acid

Brc1cnc(c(c1)B(O)O)Br Request for Quotation
Chemical Name: (2,5-dibromopyridin-3-yl)boronic acid
CAS Number: 852228-14-9
Product Number: AG004VY9(AGN-PC-01XFWY)
Synonyms:
MDL No:
Molecular Formula: C5H4BBr2NO2
Molecular Weight: 280.7098

Identification/Properties

Properties
MP:
206 °C
Storage:
Keep in dry area;2-8℃;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2,5-Dibromopyridin-3-yl)boronic acid is a versatile compound commonly used in chemical synthesis as a building block for creating various organic molecules. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, where it serves as a key component in forming carbon-carbon bonds. By incorporating (2,5-Dibromopyridin-3-yl)boronic acid into the reaction mixture, chemists can efficiently connect different functional groups together, enabling the synthesis of complex compounds with specific structures and properties. This compound's diverse applications in chemical synthesis make it a valuable tool for researchers and synthetic chemists striving to develop new materials, pharmaceuticals, and other innovative products.