CAS 1133057-98-3

[9-(2-Naphthalenyl)-9H-carbazol-3-yl]-boronic acid

Description:

[9-(2-Naphthalenyl)-9H-carbazol-3-yl]-boronic acid is an organic compound characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The structure features a carbazole moiety, which contributes to its potential as a semiconductor and in optoelectronic devices due to its planar structure and ability to facilitate charge transport. The presence of the naphthalene group enhances its aromatic character and may influence its photophysical properties, such as fluorescence. This compound is typically utilized in research related to organic electronics, sensors, and as a building block in the synthesis of more complex organic molecules. Its boronic acid functionality also allows for participation in Suzuki coupling reactions, a valuable method for forming carbon-carbon bonds in organic synthesis. Overall, this compound exhibits characteristics that make it significant in both academic research and potential industrial applications.

Formula: C₂₂H₁₆BNO₂

Synonyms:

• [9-(2-naphthalenyl)-9H-carbazole-3-yl] boronic acid

[9-(Naphthalen-2-yl)-9H-carbazol-3-yl]boronic Acid (contains varying amounts of Anhydride)

CAS: 1133057-98-3

Formula: C₂₂H₁₆BNO₂

Color and Shape: White to Light yellow powder to crystaline

Molecular weight: 337.19

Ref: 3B-N1098

(9-(Naphthalen-2-Yl)-9H-Carbazol-3-Yl)Boronic Acid

CAS: 1133057-98-3

(9-(Naphthalen-2-Yl)-9H-Carbazol-3-Yl)Boronic Acid

Purity: 97%

Molecular weight: 337.18g/mol

Ref: 54-OR1008299