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CAS 207279-32-1

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B-2,1,3-Benzoxadiazol-4-ylboronic acid

Description:
B-2,1,3-Benzoxadiazol-4-ylboronic acid is a chemical compound characterized by its unique structure, which includes a benzoxadiazole moiety and a boronic acid functional group. This compound typically exhibits properties such as good solubility in polar solvents, making it suitable for various applications in organic synthesis and materials science. The presence of the boronic acid group allows for participation in Suzuki-Miyaura cross-coupling reactions, which are essential in the formation of carbon-carbon bonds. Additionally, the benzoxadiazole unit contributes to its potential as a fluorescent probe or in the development of organic light-emitting diodes (OLEDs) due to its electronic properties. The compound may also exhibit biological activity, making it of interest in medicinal chemistry. Its stability and reactivity can vary based on environmental conditions, such as pH and temperature. Overall, B-2,1,3-Benzoxadiazol-4-ylboronic acid is a versatile compound with significant implications in both synthetic and applied chemistry.
Formula:C6H5BN2O3
InChI:InChI=1S/C6H5BN2O3/c10-7(11)4-2-1-3-5-6(4)9-12-8-5/h1-3,10-11H
InChI key:InChIKey=YLDPFKCZAMVFDF-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=2C(=NON2)C=CC1
Synonyms:
  • Boronic acid, B-2,1,3-benzoxadiazol-4-yl-
  • B-2,1,3-Benzoxadiazol-4-ylboronic acid
  • (2,1,3-Benzoxadiazol-4-yl)boronic acid
  • Boronic acid, 2,1,3-benzoxadiazol-4-yl-
  • Benzo[c][1,2,5]oxadiazol-4-ylboronic acid
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