(2-Methyl-5-pyrrolidin-1-ylsulfonyl-phenyl)boronic acid is a boronic acid derivative characterized by its unique functional groups, which include a boronic acid moiety and a sulfonamide group. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid and sulfonyl functionalities. It is often utilized in organic synthesis, particularly in Suzuki coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. The presence of the pyrrolidine ring contributes to its potential biological activity, making it of interest in medicinal chemistry. Additionally, the compound may exhibit specific reactivity towards diols, forming stable complexes, which is a characteristic feature of boronic acids. Its molecular structure allows for potential applications in drug development and materials science, particularly in the design of sensors or catalysts. As with many boronic acids, careful handling is advised due to their sensitivity to moisture and air, which can affect their stability and reactivity.

(2-methyl-5-pyrrolidin-1-ylsulfonyl-phenyl)boronic acid

871333-01-6: (2-Methyl-5-pyrrolidin-1-ylsulfonyl-phenyl)boronic acid is a boronic acid derivative characterized by its unique functional groups, which include a boronic acid moiety and a sulfonamide group. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid and sulfonyl functionalities. It is often utilized in organic synthesis, particularly in Suzuki coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. The presence of the pyrrolidine ring contributes to its potential biological activity, making it of interest in medicinal chemistry. Additionally, the compound may exhibit specific reactivity towards diols, forming stable complexes, which is a characteristic feature of boronic acids. Its molecular structure allows for potential applications in drug development and materials science, particularly in the design of sensors or catalysts. As with many boronic acids, careful handling is advised due to their sensitivity to moisture and air, which can affect their stability and reactivity.

CAS 871333-01-6

(2-methyl-5-pyrrolidin-1-ylsulfonyl-phenyl)boronic acid

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