Boronic acid, B-[2-(aminomethyl)phenyl]- (CAS 248274-03-5), is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has an aminomethyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The aminomethyl group enhances its reactivity and solubility in polar solvents, facilitating its use in coupling reactions and as a building block in the synthesis of more complex molecules. Additionally, boronic acids are known for their role in the development of boron-containing drugs and materials, particularly in the context of targeted therapies and sensor technologies. The compound's structure allows for potential interactions with biological systems, which may be explored in drug design and development. Overall, B-[2-(aminomethyl)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and applied chemistry.

Boronic acid,B-[2-(aminomethyl)phenyl]-

248274-03-5: Boronicacid, [2-(aminomethyl)phenyl]- (9CI)

(2-(Aminomethyl)phenyl)boronic acid

Boronic acid, B-[2-(aminomethyl)phenyl]-

(2-Aminomethyl)phenylboronic acid is a bifunctional molecule that has been studied for its ability to be used as a fluorescent probe. It can be used in the study of uptake, fluorescence, and transduction of cells. This compound has been shown to be useful for the study of chiral molecules due to its high degree of chirality. (2-Aminomethyl)phenylboronic acid also has a nanosized structure that is suitable for transfection efficiency and biomolecular stabilization.

CAS 248274-03-5: Boronic acid,B-[2-(aminomethyl)phenyl]-

(2-(Aminomethyl)phenyl)boronic acid

Ref: 10-F791591

Boronic acid, B-[2-(aminomethyl)phenyl]-

Ref: IN-DA002PLE

(2-(Aminomethyl)phenyl)boronic acid

Ref: 3D-FA140856

2-(Aminomethyl)phenyl boronic acid

Ref: 54-OR360234