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CAS 659731-18-7

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3-(Pyrrolidino)Phenylboronic acid

Description:
3-(Pyrrolidino)Phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a pyrrolidine moiety. This compound typically exhibits properties associated with both boronic acids and amines, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as drug development and materials science. The boronic acid group allows for participation in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. Additionally, the pyrrolidine ring contributes to the compound's solubility and reactivity, influencing its interaction with biological targets. The compound is generally stable under standard conditions but may require careful handling due to the reactivity of the boronic acid group. Its unique structure and functional properties make it a valuable intermediate in the synthesis of pharmaceuticals and other complex organic molecules.
Formula:C10H14BNO2
InChI:InChI=1/C10H14BNO2/c13-11(14)9-4-3-5-10(8-9)12-6-1-2-7-12/h3-5,8,13-14H,1-2,6-7H2
SMILES:C1CCN(C1)c1cccc(c1)B(O)O
Synonyms:
  • [3-(Pyrrolidin-1-yl)phenyl]boronic acid
  • boronic acid, B-[3-(1-pyrrolidinyl)phenyl]-
  • (3-Pyrrolidin-1-Ylphenyl)Boronic Acid
  • 3-(Pyrrolidin-1-Yl)Phenylboronic Acid
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