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CAS 362612-66-6

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[4-(thiophen-2-yl)phenyl]boronic acid

Description:
[4-(Thiophen-2-yl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is further substituted with a thiophene moiety. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity with various electrophiles due to the boronic acid group, which can participate in Suzuki coupling reactions, making it valuable in organic synthesis and materials science. The thiophene ring contributes to its electronic properties, potentially enhancing its conductivity and photophysical characteristics. Additionally, the compound may exhibit interesting interactions with biological systems, making it a candidate for applications in medicinal chemistry. Its structural features allow for the formation of coordination complexes with metals, which can be useful in catalysis. Overall, [4-(thiophen-2-yl)phenyl]boronic acid is a versatile compound with applications in organic synthesis, materials science, and potentially in pharmaceuticals.
Formula:C10H9BO2S
InChI:InChI=1/C10H9BO2S/c12-11(13)9-5-3-8(4-6-9)10-2-1-7-14-10/h1-7,12-13H
SMILES:c1cc(c2ccc(cc2)B(O)O)sc1
Synonyms:
  • 4-(2-Thienyl)Phenylboronic Acid
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