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CAS 913835-83-3

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(2-pyrrolidin-1-ylsulfonylphenyl)boronic acid

Description:
(2-Pyrrolidin-1-ylsulfonylphenyl)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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a pyrrolidine ring, which contributes to its structural complexity and may influence its reactivity and solubility. The sulfonyl group enhances the compound's polarity, potentially affecting its interactions with biological systems and its solubility in different solvents. This compound is often utilized in medicinal chemistry and materials science due to its ability to act as a building block in the synthesis of more complex molecules. Its unique combination of functional groups allows for diverse applications, including in drug development and as a reagent in organic synthesis. As with many boronic acids, it may exhibit sensitivity to moisture and air, necessitating careful handling and storage conditions to maintain its stability and efficacy.
Formula:C10H14BNO4S
InChI:InChI=1/C10H14BNO4S/c13-11(14)9-5-1-2-6-10(9)17(15,16)12-7-3-4-8-12/h1-2,5-6,13-14H,3-4,7-8H2
SMILES:c1ccc(c(c1)B(O)O)S(=O)(=O)N1CCCC1
Synonyms:
  • [2-(Pyrrolidin-1-ylsulfonyl)phenyl]boronic acid
  • Boronic acid, B-[2-(1-pyrrolidinylsulfonyl)phenyl]-
  • N-PYRROLIDINYL 2-BORONOBENZENESULFONAMIDE
  • (2-(Pyrrolidin-1-ylsulfonyl)
  • 2-(Pyrrolidin-1-ylsulphonyl)benzeneboronic acid 97%
  • 1-(2-Boronobenzenesulfonyl)pyrrolidine
  • 2-(PYRROLIDIN-1-YLSULPHONYL)BENZENEBORONIC ACID
  • 2-(Pyrrolidin-1-ylsulfonyl)benzeneboronic acid
  • [2-(1-pyrrolidinylsulfonyl)phenyl]boronic acid
  • 2-(PYRROLIDIN-1-YLSULPHONYL)BENZENEBORONIC ACID 97 USP/EP/BP
  • See more synonyms
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