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CAS 136099-65-5

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5-METHYLBENZOTHIOPHENE-2-BORONIC ACID

Description:
5-Methylbenzothiophene-2-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a methyl-substituted benzothiophene ring. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including stability and reactivity due to the boronic acid moiety. The boronic acid group allows for participation in various chemical reactions, such as Suzuki coupling, making it valuable in organic synthesis and materials science. The presence of the methyl group can influence the compound's solubility and reactivity, potentially enhancing its utility in medicinal chemistry and the development of organic electronic materials. Additionally, the thiophene ring contributes to the compound's electronic properties, which may be beneficial in applications such as organic semiconductors. Overall, 5-methylbenzothiophene-2-boronic acid is a versatile compound with significant implications in synthetic organic chemistry and materials development.
Formula:C9H9BO2S
InChI:InChI=1/C9H9BO2S/c1-6-2-3-8-7(4-6)5-9(13-8)10(11)12/h2-5,11-12H,1H3
InChI key:InChIKey=DHNHZPQPQAINDI-UHFFFAOYSA-N
SMILES:B(O)(O)C=1SC=2C(C1)=CC(C)=CC2
Synonyms:
  • (5-Methyl-1-benzothiophen-2-yl)boronic acid
  • (5-Methylbenzo[b]thien-2-yl)boronic acid
  • 5-Methyl-1-Benzothiophen-2-Ylboronic Acid
  • 5-Methylbenzo[B]Thiophene-2-Boronic Acid
  • 5-Methylbenzo[b]thiophene-2-boronic acid 97%
  • 5-Methylbenzothiphene-2-boronic acid
  • B-(5-Methylbenzo[b]thien-2-yl)boronic acid
  • Boronic acid, (5-methylbenzo[b]thien-2-yl)-
  • Boronic acid, B-(5-methylbenzo[b]thien-2-yl)-
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