Boronic acid derivatives, such as Boronic acid, B-[3-[(4-methyl-1-piperazinyl)carbonyl]phenyl]-, hydrochloride (CAS 957060-92-3), typically exhibit unique characteristics due to the presence of both boron and functional groups that enhance their reactivity and solubility. This compound features a boronic acid moiety, which is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the piperazine ring contributes to its biological activity, potentially enhancing its interaction with biological targets. As a hydrochloride salt, it is likely to be more soluble in water compared to its free base form, facilitating its use in aqueous environments. Additionally, boronic acids are often utilized in drug development due to their ability to modulate biological pathways, making this compound of interest in pharmaceutical research. Overall, the combination of boron chemistry and the piperazine structure suggests potential utility in therapeutic applications, particularly in the development of targeted therapies.

Boronic acid, B-[3-[(4-methyl-1-piperazinyl)carbonyl]phenyl]-, hydrochloride (1:1)

957060-92-3: Boronic acid, B-[3-[(4-methyl-1-piperazinyl)carbonyl]phenyl]-, hydrochloride (1:1), (3-(4-Methylpiperazine-1-carbonyl)phenyl)boronic acid hydrochloride

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CAS 957060-92-3: Boronic acid, B-[3-[(4-methyl-1-piperazinyl)carbonyl]phenyl]-, hydrochloride (1:1)

3-(4-Methylpiperazine-1-carbonyl)phenylboronic acid, HCl

Ref: 3D-FM161027

3-[(4-Methylpiperazin-1-yl)carbonyl]benzeneboronic acid hydrochloride

Ref: 54-OR3486

3-(4-Methylpiperazine-1-carbonyl)phenylboronic acid, HCl

Ref: IN-DA00IJDF