
Catalog Number	AR0038HG
Chemical Name	1,3-Benzenediboronic acid
CAS Number	4612-28-6
Molecular Formula	C6H8B2O4
Molecular Weight	165.7473
MDL Number	MFCD03092915
SMILES	OB(c1cccc(c1)B(O)O)O
NSC Number	25409

1,3-Benzenediboronic Acid, also known as m-Phenyleneboronic Acid, is a versatile building block in organic chemistry. Its unique structure featuring two boronic acid groups attached to a benzene ring makes it a valuable reagent in chemical synthesis. One of the primary applications of 1,3-Benzenediboronic Acid is in the formation of carbon-carbon and carbon-heteroatom bonds through Suzuki-Miyaura cross-coupling reactions.In the Suzuki-Miyaura cross-coupling reaction, 1,3-Benzenediboronic Acid reacts with an organic halide compound in the presence of a palladium catalyst and a base to form a new carbon-carbon bond. This reaction allows for the synthesis of biaryl compounds, which are important in the pharmaceutical industry as they are commonly found in many bioactive molecules.Furthermore, 1,3-Benzenediboronic Acid can also be utilized in the construction of dendrimers, which are highly branched macromolecules with applications in drug delivery systems, materials science, and nanotechnology. By incorporating 1,3-Benzenediboronic Acid units into the dendrimer structure, it is possible to modulate the properties and functionality of these complex molecules.Overall, the capability of 1,3-Benzenediboronic Acid to participate in cross-coupling reactions and dendrimer synthesis highlights its significance as a key intermediate in chemical synthesis, making it an indispensable tool for organic chemists seeking to access diverse molecular architectures.

Boronic acid, B,B′-1,4-phenylenebis-, homopolymer

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1,3-Benzenediboronic acid

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Packsize	Purity	Price	Availability
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