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CAS 874219-52-0

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B-[4-Methoxy-3-(1-pyrrolidinylsulfonyl)phenyl]boronic acid

Description:
B-[4-Methoxy-3-(1-pyrrolidinylsulfonyl)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. This compound features a phenyl ring substituted with a methoxy group and a pyrrolidinylsulfonyl moiety, contributing to its potential biological activity. The presence of the pyrrolidine ring suggests possible interactions with biological targets, making it of interest in medicinal chemistry. Boronic acids are often utilized in various applications, including drug development, particularly in the context of protease inhibitors and in the synthesis of complex organic molecules through Suzuki coupling reactions. The compound's solubility, stability, and reactivity can be influenced by the substituents on the phenyl ring and the boronic acid group, which can affect its utility in research and pharmaceutical applications. Overall, this compound exemplifies the diverse functionalities that can be achieved through careful molecular design in organic chemistry.
Formula:C11H16BNO5S
InChI:InChI=1S/C11H16BNO5S/c1-18-10-5-4-9(12(14)15)8-11(10)19(16,17)13-6-2-3-7-13/h4-5,8,14-15H,2-3,6-7H2,1H3
InChI key:InChIKey=CMUQRJVOEZOCJL-UHFFFAOYSA-N
SMILES:S(=O)(=O)(C1=C(OC)C=CC(B(O)O)=C1)N2CCCC2
Synonyms:
  • B-[4-Methoxy-3-(1-pyrrolidinylsulfonyl)phenyl]boronic acid
  • Boronic acid, [4-methoxy-3-(1-pyrrolidinylsulfonyl)phenyl]-
  • [4-Methoxy-3-[(pyrrolidin-1-yl)sulfonyl]phenyl]boronic acid
  • Boronic acid, B-[4-methoxy-3-(1-pyrrolidinylsulfonyl)phenyl]-
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