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CAS 389621-81-2

:

4-(Pyrrolidine-1-carbonyl)phenylboronic acid

Description:
4-(Pyrrolidine-1-carbonyl)phenylboronic acid, with the CAS number 389621-81-2, is an organic compound that features a boronic acid functional group attached to a phenyl ring, which is further substituted with a pyrrolidine-1-carbonyl moiety. This compound is characterized by its ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and materials science. The presence of the boronic acid group allows for potential interactions in biological systems, particularly in the development of drug candidates targeting specific enzymes or receptors. Additionally, the pyrrolidine ring contributes to the compound's steric and electronic properties, influencing its reactivity and solubility. Typically, compounds like this are studied for their role in drug delivery systems, as well as in the synthesis of complex organic molecules through cross-coupling reactions. Overall, 4-(Pyrrolidine-1-carbonyl)phenylboronic acid exemplifies the versatility of boronic acids in organic synthesis and their significance in pharmaceutical research.
Formula:C11H14BNO3
InChI:InChI=1/C11H14BNO3/c14-11(13-7-1-2-8-13)9-3-5-10(6-4-9)12(15)16/h3-6,15-16H,1-2,7-8H2
SMILES:C1CCN(C1)C(=O)c1ccc(cc1)B(O)O
Synonyms:
  • [4-(Pyrrolidin-1-Ylcarbonyl)Phenyl]Boronic Acid
  • 4-(Pyrrolidine-1-Carbonyl)Benzeneboronic Acid
  • 4-(Pyrrolidine-1-carbonyl)-phenyl boronic acid:
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