2-(Diphenylamino)phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a diphenylamino group. This compound typically exhibits properties associated with both boronic acids and amines, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis and materials science. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds. Additionally, the diphenylamino moiety can enhance the electronic properties of the compound, potentially making it useful in organic electronics or as a fluorescent probe. The compound is likely to be a solid at room temperature and may exhibit solubility in polar organic solvents. Its reactivity and functional versatility make it a valuable building block in the development of complex organic molecules and materials. Safety data should be consulted for handling and storage, as with all chemical substances.

2-(diphenylamino)phenylboronic acid

934169-37-6: 2-(Diphenylamino)phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a diphenylamino group. This compound typically exhibits properties associated with both boronic acids and amines, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis and materials science. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds. Additionally, the diphenylamino moiety can enhance the electronic properties of the compound, potentially making it useful in organic electronics or as a fluorescent probe. The compound is likely to be a solid at room temperature and may exhibit solubility in polar organic solvents. Its reactivity and functional versatility make it a valuable building block in the development of complex organic molecules and materials. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 934169-37-6

2-(diphenylamino)phenylboronic acid

(2-(Diphenylamino)phenyl)boronic acid

Ref: 54-OR1074180