CAS 1029439-56-2

4-(N-Phenylaminomethyl)Phenylboronic Acid

Description:

4-(N-Phenylaminomethyl)Phenylboronic Acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical applications, including drug development and materials science. This compound features a phenyl group substituted with an aminomethyl group, enhancing its reactivity and potential for forming complexes with biomolecules. The boronic acid moiety contributes to its acidity and reactivity, allowing it to participate in Suzuki-Miyaura cross-coupling reactions, which are pivotal in synthesizing complex organic molecules. Additionally, the presence of the phenylamine group may impart specific electronic properties, influencing its behavior in biological systems. The compound is typically solid at room temperature and may exhibit solubility in polar organic solvents. Its applications may extend to areas such as sensor development, where its ability to interact with specific biomolecules can be harnessed for detection purposes. Overall, 4-(N-Phenylaminomethyl)Phenylboronic Acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.

N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)aniline

CAS: 1029439-56-2

Formula: C₁₉H₂₄BNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 309.2104

Ref: IN-DA003SBA

[4-(Phenylaminomethyl)phenyl]-boronic acid pinacol ester

CAS: 1029439-56-2

[4-(Phenylaminomethyl)phenyl]-boronic acid pinacol ester

Purity: 98%

Molecular weight: 309.21g/mol

Ref: 54-OR303423

N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)aniline

CAS: 1029439-56-2

Purity: 98%

Molecular weight: 309.2200012

Ref: 10-F694080