
CAS 1256355-38-0
:3,4-DIBROMOTHIOPHEN-2-YLBORONIC ACID
Description:
3,4-Dibromothiophen-2-ylboronic acid is an organoboron compound characterized by the presence of both bromine and boronic acid functional groups attached to a thiophene ring. This compound typically exhibits a yellow to brown color and is soluble in polar organic solvents. The presence of bromine atoms enhances its reactivity, making it useful in cross-coupling reactions, particularly in the synthesis of complex organic molecules. The boronic acid group allows for the formation of boronate esters, which are valuable intermediates in organic synthesis. Additionally, the thiophene ring contributes to the compound's electronic properties, making it suitable for applications in organic electronics and materials science. Its unique structure and functional groups enable it to participate in various chemical reactions, including Suzuki coupling, which is widely used in the formation of carbon-carbon bonds. Safety data should be consulted for handling and storage, as organoboron compounds can pose health risks if not managed properly.
Formula:C4H3BBr2O2S
Synonyms:- Boronic acid, B-(3,4-dibromo-2-thienyl)-
- 3,4-dibromothiophene-2-boronic acid
- 3,4-DIBROMOTHIOPHEN-2-YLBORONIC ACID
- 3,4-Dibromothiophen-2-boronic acid
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Found 3 products.
3,4-Dibromothiophen-2-boronic acid
CAS:Formula:C4H3BBr2O2SPurity:96%Color and Shape:SolidMolecular weight:285.74943,4-Dibromothiophen-2-boronic acid
CAS:<p>3,4-Dibromothiophen-2-boronic acid</p>Purity:96%Molecular weight:285.75g/mol


