Boronic acid, specifically the compound known as B-[3-[[[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 can enhance solubility and stability in aqueous solutions. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, and may exhibit properties that allow for interactions with biological targets, making them of interest in drug development. The specific structure of this compound suggests potential applications in areas such as cancer therapy or as a biochemical probe, although detailed biological activity would require further investigation. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential toxicity.

Boronic acid,B-[3-[[[2-(1-pyrrolidinyl)ethyl]amino]carbonyl]phenyl]-, hydrochloride (1:1)

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3-[(2-Pyrrolidin-1-ylethyl)carbamoyl]benzeneboronic acid hydrochloride

3-(2-(Pyrrolidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl

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CAS 957061-03-9: Boronic acid,B-[3-[[[2-(1-pyrrolidinyl)ethyl]amino]carbonyl]phenyl]-, hydrochloride (1:1)

3-[(2-Pyrrolidin-1-ylethyl)carbamoyl]benzeneboronic acid hydrochloride

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3-(2-(Pyrrolidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl

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3-(2-(Pyrrolidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl

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