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4612-28-6

1,3-Benzenediboronic acid

Catalog#: AR0038HG  |   CAS#: 4612-28-6  |   MDL#: MFCD03092915  |   MF: C6H8B2O4  |   MW: 165.7473

Packsize Purity Price Availability Quantity
250mg 97% $3.00 Global Stock Buy Now Add To Cart
1g 97% $7.00 Global Stock Buy Now Add To Cart
5g 97% $31.00 Global Stock Buy Now Add To Cart
10g 97% $61.00 Global Stock Buy Now Add To Cart
25g 97% $150.00 Global Stock Buy Now Add To Cart
100g 97% $600.00 Global Stock Buy Now Add To Cart
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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.
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