Boronic acid, specifically the compound known as B-[4-[[[2-(1-pyrrolidinyl)ethyl]amino]carbonyl]phenyl]-, hydrochloride (1:1), is a chemical substance characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a pyrrolidine moiety, contributing to its potential biological activity, particularly in medicinal chemistry. The presence of the hydrochloride indicates that it is a salt form, which often enhances solubility in aqueous solutions, making it suitable for various applications, including drug formulation. The structure suggests potential interactions with biological targets, possibly influencing enzyme activity or serving as a building block in organic synthesis. Additionally, boronic acids are recognized for their role in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. Overall, this compound's unique structural features and functional groups suggest it may have applications in pharmaceuticals, particularly in the development of therapeutic agents.

Boronic acid,B-[4-[[[2-(1-pyrrolidinyl)ethyl]amino]carbonyl]phenyl]-, hydrochloride (1:1)

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4-(2-(Pyrrolidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl

4-[(2-Pyrrolidin-1-ylethyl)carbamoyl]benzeneboronic acid hydrochloride

CAS 957060-70-7: Boronic acid,B-[4-[[[2-(1-pyrrolidinyl)ethyl]amino]carbonyl]phenyl]-, hydrochloride (1:1)

4-(2-(Pyrrolidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl

Ref: 3D-FP161024

4-[(2-Pyrrolidin-1-ylethyl)carbamoyl]benzeneboronic acid hydrochloride

Ref: 54-OR3264

Boronic acid,B-[4-[[[2-(1-pyrrolidinyl)ethyl]amino]carbonyl]phenyl]-, hydrochloride (1:1)

Ref: IN-DA00IJDD