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CAS 1218790-70-5

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B-[6-(Cyclopentylthio)-3-pyridinyl]boronic acid

Description:
B-[6-(Cyclopentylthio)-3-pyridinyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that features a cyclopentylthio substituent. This compound typically exhibits properties associated with 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 presence of the cyclopentylthio group enhances its lipophilicity and may influence its biological activity, potentially making it a candidate for drug development. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds in organic synthesis. The compound's solubility, stability, and reactivity can vary based on the specific conditions, such as pH and solvent, which are crucial for its application in research and industry. Overall, B-[6-(Cyclopentylthio)-3-pyridinyl]boronic acid represents a versatile structure in the field of chemistry.
Formula:C10H14BNO2S
InChI:InChI=1S/C10H14BNO2S/c13-11(14)8-5-6-10(12-7-8)15-9-3-1-2-4-9/h5-7,9,13-14H,1-4H2
InChI key:InChIKey=PDWYJFZHFSBLOZ-UHFFFAOYSA-N
SMILES:S(C1=CC=C(B(O)O)C=N1)C2CCCC2
Synonyms:
  • B-[6-(Cyclopentylthio)-3-pyridinyl]boronic acid
  • Boronic acid, B-[6-(cyclopentylthio)-3-pyridinyl]-
  • 2-(Cyclopentylthio)pyridine-5-boronic acid
  • 6-(Cyclopentylthio)pyridin-3-ylboronic acid
  • [6-(Cyclopentylsulfanyl)pyridin-3-yl]boronic acid
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