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CAS 723281-53-6

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[3-(pyrrolidin-1-ylcarbonyl)phenyl]boronic acid

Description:
[3-(Pyrrolidin-1-ylcarbonyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a pyrrolidin-1-ylcarbonyl group, contributing to its structural complexity and potential biological activity. Boronic acids are typically polar and can exhibit solubility in polar solvents, while the presence of the pyrrolidine moiety may enhance its lipophilicity and biological interactions. This compound may serve as a building block in the synthesis of more complex molecules or as a ligand in catalysis. Additionally, its unique structure may impart specific reactivity patterns, making it of interest in the development of pharmaceuticals or agrochemicals. As with many boronic acids, it is essential to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C11H14BNO3
InChI:InChI=1/C11H14BNO3/c14-11(13-6-1-2-7-13)9-4-3-5-10(8-9)12(15)16/h3-5,8,15-16H,1-2,6-7H2
SMILES:C1CCN(C1)C(=O)c1cccc(c1)B(O)O
Synonyms:
  • [3-(1-Pyrrolidinylcarbonyl)phenyl]boronic acid
  • Boronic acid, B-[3-(1-pyrrolidinylcarbonyl)phenyl]-
  • 3-Pyrrolidinylcarbonylphenylboronicacid
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