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CAS 1044210-58-3

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B-(5-Cyclopropyl-3-pyridinyl)boronic acid

Description:
B-(5-Cyclopropyl-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 cyclopropyl substituent. 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 cyclopropyl group contributes to the compound's unique steric and electronic properties, potentially influencing its reactivity and interactions with biological targets. Additionally, the presence of the pyridine ring can enhance solubility in polar solvents and may participate in hydrogen bonding. B-(5-Cyclopropyl-3-pyridinyl)boronic acid may also exhibit specific biological activities, making it of interest in drug discovery and development. Its structural features suggest potential applications in the development of inhibitors or modulators of biological pathways, particularly in the context of cancer research and other therapeutic areas. As with many boronic acids, careful handling and storage are recommended due to their sensitivity to moisture and air.
Formula:C8H10BNO2
InChI:InChI=1S/C8H10BNO2/c11-9(12)8-3-7(4-10-5-8)6-1-2-6/h3-6,11-12H,1-2H2
InChI key:InChIKey=MLRXPBXNCWRWOM-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(=CN=C1)C2CC2
Synonyms:
  • B-(5-Cyclopropyl-3-pyridinyl)boronic acid
  • Boronic acid, B-(5-cyclopropyl-3-pyridinyl)-
  • (5-cyclopropyl-3-pyridyl)boronic acid
  • 5-Cyclopropylpyridine-3-Boronic acid
  • 5-CYCLOPROPYLPYRIDIN-3-YLBORONIC ACID
  • 5-Cyclopropylpyridin-3-ylboronic&nbsp
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