9-(Prop-2-yn-1-yl)-9H-carbazole, with the CAS number 4282-77-3, is an organic compound that belongs to the class of carbazoles, which are polycyclic aromatic compounds featuring a nitrogen atom in their structure. This compound is characterized by its fused ring system, consisting of a carbazole core with a prop-2-yn-1-yl substituent at the 9-position. The presence of the alkyne group (prop-2-yn-1-yl) imparts unique reactivity, making it suitable for various synthetic applications, particularly in organic synthesis and materials science. The compound exhibits properties typical of aromatic systems, such as stability and potential for π-π stacking interactions. Additionally, due to the presence of the alkyne functional group, it may participate in reactions such as cycloadditions or coupling reactions. Its solubility and stability can vary depending on the solvent and environmental conditions. Overall, 9-(prop-2-yn-1-yl)-9H-carbazole is of interest in research fields exploring organic electronics, photonics, and advanced materials.

9-(prop-2-yn-1-yl)-9H-carbazole

4282-77-3: 9-(2-Propynyl)-9H-carbazole, 9H-Carbazole, 9-(2-propyn-1-yl)-, 9-Prop-2-ynyl-9H-carbazole, Carbazole, 9-(2-propynyl)-,  9-(Prop-2-yn-1-yl)-9H-carbazole

9-(Prop-2-yn-1-yl)-9H-carbazole is a monomer that has been shown to be insoluble, diffraction, and regioselective. Its copolymerization with 1,3-diphenylpropane yields polymers with high molecular weight. 9-(Prop-2-yn-1-yl)-9H-carbazole can be polymerized by the addition of sulfate ions, which can also act as a catalyst for the polymerization process. Copolymers of 9-(Prop-2-yn-1-yl)-9H-carbazole have been shown to possess photoconductive properties. This monomer has also been shown to be an effective catalyst for the 1,3 dipolar cycloaddition reaction.

CAS 4282-77-3: 9-(prop-2-yn-1-yl)-9H-carbazole

9-(Prop-2-yn-1-yl)-9H-carbazole

Ref: 3D-EAA28277

3-(N-CARBAZOLYL)PROPYNE

Ref: IN-DA00CHPT

9-(Prop-2-yn-1-yl)-9H-carbazole

Ref: 10-F517824

9-(Prop-2-Yn-1-Yl)-9H-Carbazole

Ref: 54-OR1012119