2,1,3-Benzoxadiazol-5-yl-boronic acid is an organic compound characterized by the presence of a benzoxadiazole moiety and a boronic acid functional group. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar solvents due to the presence of the boronic acid group. The benzoxadiazole structure contributes to its electronic properties, often making it useful in fluorescence applications and as a building block in organic synthesis. The boronic acid functionality allows for reversible covalent bonding with diols, making it valuable in various chemical reactions, including Suzuki coupling reactions, which are essential in the synthesis of complex organic molecules. Additionally, this compound may exhibit biological activity, making it of interest in medicinal chemistry. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its application in research and industry. Overall, 2,1,3-benzoxadiazol-5-yl-boronic acid is a versatile compound with significant utility in both synthetic and applied chemistry.

2,1,3-Benzoxadiazol-5-yl-boronic Acid

426268-09-9: Benzo[c][1,2,5]oxadiazole-5-boronic acid, Benzo[c][1,2,5]oxadiazol-5-ylboronicacid

2,1,3-Benzoxadiazole-5-boronic acid

Benzo[c][1,2,5]oxadiazol-5-ylboronic acid

BENZO[C][1,2,5]OXADIAZOLE-5-BORONIC ACID

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CAS 426268-09-9: 2,1,3-Benzoxadiazol-5-yl-boronic Acid

2,1,3-Benzoxadiazole-5-boronic acid

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Benzo[c][1,2,5]oxadiazol-5-ylboronic acid

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BENZO[C][1,2,5]OXADIAZOLE-5-BORONIC ACID

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Benzo[c][1,2,5]oxadiazol-5-ylboronic acid

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