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CAS 306934-95-2

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(5-Phenylthien-2-yl)boronic acid

Description:
(5-Phenylthien-2-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a thienyl ring that is further substituted with a phenyl group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The thienyl moiety contributes to its aromatic character and potential electronic properties, while the phenyl group can enhance its stability and solubility in organic solvents. (5-Phenylthien-2-yl)boronic acid is often utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, its boronic acid functionality allows for potential applications in drug development, particularly in the design of inhibitors for certain enzymes. Overall, this compound is notable for its versatility in synthetic chemistry and its role in the development of complex organic molecules.
Formula:C10H9BO2S
InChI:InChI=1S/C10H9BO2S/c12-11(13)10-7-6-9(14-10)8-4-2-1-3-5-8/h1-7,12-13H
InChI key:InChIKey=RBSMKSPHBJFXCJ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1SC(=CC1)C2=CC=CC=C2
Synonyms:
  • (2-Phenylthien-5-yl)boronic acid
  • (5-Phenyl-2-thienyl)boronic acid
  • (5-Phenylthien-2-yl)boronic acid
  • (5-Phenylthiophen-2-Yl)Boronic Acid
  • 2-Phenyl-5-thiopheneboronic acid
  • 2-Phenythiophen-5-Ylboronic Acid
  • 5-Phenyl-2-thiopheneboronic acid
  • B-(5-Phenyl-2-thienyl)boronic acid
  • Boronic acid, (5-phenyl-2-thienyl)-
  • boronic acid, B-(5-phenyl-2-thienyl)-
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