[4-(Thiazolidine-3-carbonyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a thiazolidine-3-carbonyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The thiazolidine ring contributes to its structural complexity and may influence its biological activity, potentially offering therapeutic benefits in areas like diabetes and cancer research. The compound is likely to be a solid at room temperature, with solubility in polar solvents, and may exhibit moderate stability under standard laboratory conditions. Its reactivity can be attributed to the boron atom, which can participate in various chemical reactions, including cross-coupling reactions and ligand formation. Overall, [4-(thiazolidine-3-carbonyl)phenyl]boronic acid represents a valuable scaffold in the development of new chemical entities.

[4-(thiazolidine-3-carbonyl)phenyl]boronic acid

850589-33-2: [4-(Thiazolidine-3-carbonyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a thiazolidine-3-carbonyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The thiazolidine ring contributes to its structural complexity and may influence its biological activity, potentially offering therapeutic benefits in areas like diabetes and cancer research. The compound is likely to be a solid at room temperature, with solubility in polar solvents, and may exhibit moderate stability under standard laboratory conditions. Its reactivity can be attributed to the boron atom, which can participate in various chemical reactions, including cross-coupling reactions and ligand formation. Overall, [4-(thiazolidine-3-carbonyl)phenyl]boronic acid represents a valuable scaffold in the development of new chemical entities.

CAS 850589-33-2

[4-(thiazolidine-3-carbonyl)phenyl]boronic acid

4-(THIAZOLINE-3-CARBONYL)BENZENEBORONIC ACID

Ref: IN-DA008GT1

4-(1,3-Thiazolidin-3-ylcarbonyl)benzeneboronic acid

Ref: 54-OR4126

(4-(Thiazolidine-3-carbonyl)phenyl)boronic acid

Ref: 10-F691616