Description:(2-BOC-aminophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a tert-butyloxycarbonyl (BOC) protecting group attached to an amino group on a phenyl ring. This compound typically exhibits properties such as being a white to off-white solid, soluble in organic solvents like dichloromethane and dimethyl sulfoxide, and having limited solubility in water due to its hydrophobic BOC group. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. The BOC group serves as a protective group for the amine, facilitating selective reactions and subsequent deprotection under mild acidic conditions. This compound is often utilized in the development of pharmaceuticals and agrochemicals, as well as in materials science for the synthesis of boron-containing polymers. Its reactivity and functional versatility make it an important building block in synthetic organic chemistry.
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