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Atomfair 2-(9H-Carbazol-9-yl)ethyl acrylate C17H15NO2

Description 2-(9H-Carbazol-9-yl)ethyl acrylate (CAS No. 6915-68-0) is a high-purity organic compound with the molecular formula C17H15NO2. This specialized acrylate derivative features a carbazole moiety, known for its photoconductive and electroluminescent properties, coupled with an ethyl acrylate group for polymerization versatility. Ideal for advanced material science applications, this compound is rigorously tested for consistency, ensuring optimal performance in photoresists, OLEDs, and functional polymers. Supplied as a crystalline solid or solution (upon request), it is packaged under inert conditions to maintain stability. Suitable for researchers in organic electronics, polymer chemistry, and nanotechnology.

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Description

Description

2-(9H-Carbazol-9-yl)ethyl acrylate (CAS No. 6915-68-0) is a high-purity organic compound with the molecular formula C17H15NO2. This specialized acrylate derivative features a carbazole moiety, known for its photoconductive and electroluminescent properties, coupled with an ethyl acrylate group for polymerization versatility. Ideal for advanced material science applications, this compound is rigorously tested for consistency, ensuring optimal performance in photoresists, OLEDs, and functional polymers. Supplied as a crystalline solid or solution (upon request), it is packaged under inert conditions to maintain stability. Suitable for researchers in organic electronics, polymer chemistry, and nanotechnology.

  • CAS No: 6915-68-0
  • Molecular Formula: C17H15NO2
  • Molecular Weight: 265.31
  • Exact Mass: 265.110278721
  • Monoisotopic Mass: 265.110278721
  • IUPAC Name: 2-carbazol-9-ylethyl prop-2-enoate
  • SMILES: C=CC(=O)OCCN1C2=CC=CC=C2C3=CC=CC=C31
  • Synonyms: 2-(9H-Carbazol-9-yl)ethyl acrylate, 6915-68-0, DTXSID50391339, DTXCID50342200, 622-125-5

Application

2-(9H-Carbazol-9-yl)ethyl acrylate is widely used in the synthesis of photoactive polymers for organic light-emitting diodes (OLEDs) and photovoltaic devices. Its carbazole group enhances charge transport properties, making it valuable in optoelectronic materials. The acrylate functionality allows for facile incorporation into copolymer systems via radical polymerization. Researchers also utilize it to develop advanced photoresists for microfabrication due to its UV sensitivity. Additionally, it serves as a key monomer in creating electrochromic or conductive thin films.

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