[4-(1-Pyrrolidin-1-ylethyl)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 pyrrolidine moiety, contributing to its potential biological activity and utility in medicinal chemistry. The boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis for constructing complex molecules. It is typically a white to off-white solid and is soluble in polar organic solvents. The compound may exhibit properties such as moderate stability under ambient conditions, but it can be sensitive to moisture due to the presence of the boronic acid group. Its applications may extend to drug development, particularly in the design of inhibitors for various biological targets, owing to the structural versatility provided by the pyrrolidine and phenyl components. As with many boronic acids, careful handling and storage are recommended to maintain its integrity and reactivity.

[4-(1-pyrrolidin-1-ylethyl)phenyl]boronic acid

868395-81-7: [4-(1-Pyrrolidin-1-ylethyl)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 pyrrolidine moiety, contributing to its potential biological activity and utility in medicinal chemistry. The boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis for constructing complex molecules. It is typically a white to off-white solid and is soluble in polar organic solvents. The compound may exhibit properties such as moderate stability under ambient conditions, but it can be sensitive to moisture due to the presence of the boronic acid group. Its applications may extend to drug development, particularly in the design of inhibitors for various biological targets, owing to the structural versatility provided by the pyrrolidine and phenyl components. As with many boronic acids, careful handling and storage are recommended to maintain its integrity and reactivity.

CAS 868395-81-7

[4-(1-pyrrolidin-1-ylethyl)phenyl]boronic acid

Boronic acid, [4-[1-(1-pyrrolidinyl)ethyl]phenyl]-

Ref: IN-DA00IE86

4-(1-Pyrrolidinoethyl)phenylboronic acid

Ref: 54-OR361586

[4-(1-pyrrolidin-1-ylethyl)phenyl]boronic acid

Ref: 10-F309522