(4-Pyrrolidin-1-ylphenyl)boronic acid hydrochloride is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and a pyrrolidine moiety. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and methanol, which is a common trait for boronic acids due to their ability to form hydrogen bonds. The presence of the boronic acid functional group allows for potential applications in organic synthesis, particularly in Suzuki coupling reactions, which are vital for forming carbon-carbon bonds. Additionally, the hydrochloride form indicates that the compound is protonated, enhancing its solubility and stability in aqueous environments. This compound may also exhibit biological activity, making it of interest in medicinal chemistry. Its unique structure allows for interactions with various biological targets, potentially leading to therapeutic applications. As with many boronic acids, care should be taken in handling due to their reactivity and potential environmental impact.

(4-pyrrolidin-1-ylphenyl)boronic acid hydrochloride

229009-41-0: 4-(Pyrrolidino)phenylboronic acid, (4-Pyrrolidin-1-Ylphenyl)Boronic Acid

CAS 229009-41-0: (4-pyrrolidin-1-ylphenyl)boronic acid hydrochloride

(4-Pyrrolidin-1-ylphenyl)boronic acid

Ref: 54-OR360044

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

Ref: IN-DA002LF5

(4-Pyrrolidin-1-ylphenyl)boronic acid

Ref: 3D-EJA00941

(4-(Pyrrolidin-1-yl)phenyl)boronic acid

Ref: 10-F609222