
Catalog Number	AR003FNN
Chemical Name	2-(9H-carbazolyl)ethylboronic acid pinacol ester
CAS Number	608534-41-4
Molecular Formula	C20H24BNO2
Molecular Weight	321.2211
MDL Number	MFCD03788738
SMILES	CC1(C)OB(OC1(C)C)CCn1c2ccccc2c2c1cccc2

9-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)ethyl)-9H-carbazole, also known as $name$, is a versatile compound used in chemical synthesis as a key building block for the formation of various organic molecules. Its unique structure allows for precise manipulation and control of chemical reactions, making it a valuable tool in the creation of complex organic compounds.One of the main applications of $name$ in chemical synthesis is its use as a coupling partner in Suzuki-Miyaura cross-coupling reactions. This reaction involves the coupling of an aryl or vinyl halide with an organoboron compound in the presence of a palladium catalyst to form a new carbon-carbon bond. $name$ serves as the boron-containing component in this reaction, enabling the selective formation of biaryl compounds with high efficiency and selectivity.Additionally, $name$ can also be employed in the synthesis of functionalized carbazoles, which are important scaffolds in organic chemistry due to their diverse biological and optoelectronic properties. By utilizing $name$ as a starting material, chemists can access a wide range of substituted carbazole derivatives through various synthetic transformations, offering new opportunities for the development of innovative materials and pharmaceuticals.