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CAS 871329-61-2

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B-[3-(1-Pyrrolidinylsulfonyl)phenyl]boronic acid

Description:
B-[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 and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a pyrrolidinylsulfonyl group, which enhances its solubility and reactivity. This structure contributes to its potential applications in drug discovery, particularly in the development of protease inhibitors and other therapeutic agents. The boronic acid moiety allows for the formation of boronate esters, making it useful in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for constructing carbon-carbon bonds. Additionally, the presence of the sulfonyl group may impart unique electronic properties, influencing the compound's reactivity and interaction with biological targets. Overall, B-[3-(1-Pyrrolidinylsulfonyl)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C10H14BNO4S
InChI:InChI=1S/C10H14BNO4S/c13-11(14)9-4-3-5-10(8-9)17(15,16)12-6-1-2-7-12/h3-5,8,13-14H,1-2,6-7H2
InChI key:InChIKey=RCRUXZHMXFQVRF-UHFFFAOYSA-N
SMILES:S(=O)(=O)(C1=CC(B(O)O)=CC=C1)N2CCCC2
Synonyms:
  • Boronic acid, B-[3-(1-pyrrolidinylsulfonyl)phenyl]-
  • B-[3-(1-Pyrrolidinylsulfonyl)phenyl]boronic acid
  • 3-(Pyrrolidinosulfonyl)phenylboronic acid
  • Boronic acid, [3-(1-pyrrolidinylsulfonyl)phenyl]-
  • [3-[(Pyrrolidin-1-yl)sulfonyl]phenyl]boronic acid
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