(5-boronopyridin-3-yl)boronic acid


Chemical Name: (5-boronopyridin-3-yl)boronic acid
CAS Number: 1012085-48-1
Product Number: AG0003YR(AGN-PC-0LGF7O)
Synonyms:
MDL No:
Molecular Formula: C5H7B2NO4
Molecular Weight: 166.7354

Identification/Properties


Safety Information


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

NMR Spectrum


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Chemical Structure



Pyridine-3,5-diyldiboronic acid is a versatile chemical compound that plays a crucial role in organic synthesis. As a boronic acid derivative, it possesses unique properties that make it a valuable reagent in various chemical reactions. One of its primary applications lies in cross-coupling reactions, particularly in the formation of carbon-carbon (C-C) and carbon-heteroatom bonds.In organic synthesis, Pyridine-3,5-diyldiboronic acid acts as a key component in Suzuki-Miyaura coupling reactions, which are widely utilized for the construction of biaryl compounds. This process involves the coupling of an aryl halide or pseudohalide with an organic boronic acid derivative, such as Pyridine-3,5-diyldiboronic acid, under the catalytic influence of a transition metal complex, typically palladium. The resulting product is a biaryl compound with high regio- and stereo-selectivity.Moreover, Pyridine-3,5-diyldiboronic acid can also participate in other types of cross-coupling reactions, such as Sonogashira and Heck reactions, further expanding its utility in organic synthesis. These transformations allow for the efficient construction of complex molecular structures, making Pyridine-3,5-diyldiboronic acid an indispensable tool for chemists working in the field of medicinal chemistry, material science, and agrochemical research.