4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline hydrochloride is a chemical compound characterized by its unique structure, which includes a boron-containing dioxaborolane moiety attached to an aniline group. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the hydrochloride salt form. The dioxaborolane group is known for its reactivity in various organic transformations, particularly in cross-coupling reactions, making this compound potentially useful in synthetic organic chemistry. The presence of the aniline moiety contributes to its basicity and potential for further functionalization. Additionally, the tetramethyl substituents enhance the stability of the boron center and may influence the compound's reactivity and solubility. Safety data should be consulted, as with any chemical, to understand its handling and potential hazards. Overall, this compound represents a versatile building block in the field of organic synthesis and materials science.

4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)aniline hydrochloride

616227-14-6: 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline hydrochloride is a chemical compound characterized by its unique structure, which includes a boron-containing dioxaborolane moiety attached to an aniline group. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the hydrochloride salt form. The dioxaborolane group is known for its reactivity in various organic transformations, particularly in cross-coupling reactions, making this compound potentially useful in synthetic organic chemistry. The presence of the aniline moiety contributes to its basicity and potential for further functionalization. Additionally, the tetramethyl substituents enhance the stability of the boron center and may influence the compound's reactivity and solubility. Safety data should be consulted, as with any chemical, to understand its handling and potential hazards. Overall, this compound represents a versatile building block in the field of organic synthesis and materials science.

4-Aminophenylboronic acid, pinacol ester, HCl

4-Aminobenzeneboronic acid, pinacol ester hydrochloride

CAS 616227-14-6

4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)aniline hydrochloride

4-Aminophenylboronic acid, pinacol ester, HCl

Ref: IN-DA00EL87

4-Aminobenzeneboronic acid, pinacol ester hydrochloride

Ref: 54-OR10341