Boronic acid, specifically the compound with the name "Boronic acid, B-[4-[(4-methyl-1-piperazinyl)carbonyl]phenyl]-" and CAS number 374927-12-5, is characterized by its boron-containing functional group, which is typically known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a piperazine moiety, which enhances its biological activity and solubility. The presence of the carbonyl group linked to the piperazine suggests potential reactivity and interaction with various biological targets, making it of interest in medicinal chemistry. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, and can serve as intermediates in the development of pharmaceuticals. Additionally, the piperazine ring may contribute to the compound's pharmacokinetic properties, such as improved membrane permeability and bioavailability. Overall, this compound exemplifies the versatility of boronic acids in both synthetic and medicinal chemistry applications.

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

374927-12-5: Boronicacid, [4-[(4-methyl-1-piperazinyl)carbonyl]phenyl]- (9CI), (4-((4-Methylpiperazin-1-yl)carbonyl)phenyl)boronic acid

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CAS 374927-12-5: Boronic acid,B-[4-[(4-methyl-1-piperazinyl)carbonyl]phenyl]-

4-(4-Methylpiperazine-1-carbonyl)phenylboronic acid

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4-(4-Methylpiperazine-1-carbonyl)phenylboronic acid

Ref: 10-F609195

Boronic acid, [4-[(4-methyl-1-piperazinyl)carbonyl]phenyl]- (9CI)

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