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Atomfair 9-(4,6-Dichloro-1,3,5-triazin-2-yl)-9H-carbazole C15H8Cl2N4

Description 9-(4,6-Dichloro-1,3,5-triazin-2-yl)-9H-carbazole (CAS No. 24209-95-8) is a high-purity organic compound with the molecular formula C15H8Cl2N4. This specialized chemical features a carbazole moiety linked to a reactive dichlorotriazine group, making it a valuable intermediate in synthetic organic chemistry and materials science. Its unique structure enables applications in pharmaceuticals, agrochemicals, and advanced material synthesis. The compound is supplied as a fine crystalline powder with ??95% purity (HPLC), ensuring consistency for research and industrial use. Proper storage in a cool, dry environment under inert conditions is recommended to maintain stability.

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Description

Description

9-(4,6-Dichloro-1,3,5-triazin-2-yl)-9H-carbazole (CAS No. 24209-95-8) is a high-purity organic compound with the molecular formula C15H8Cl2N4. This specialized chemical features a carbazole moiety linked to a reactive dichlorotriazine group, making it a valuable intermediate in synthetic organic chemistry and materials science. Its unique structure enables applications in pharmaceuticals, agrochemicals, and advanced material synthesis. The compound is supplied as a fine crystalline powder with ??95% purity (HPLC), ensuring consistency for research and industrial use. Proper storage in a cool, dry environment under inert conditions is recommended to maintain stability.

  • CAS No: 24209-95-8
  • Molecular Formula: C15H8Cl2N4
  • Molecular Weight: 315.2
  • Exact Mass: 314.0126017
  • Monoisotopic Mass: 314.0126017
  • IUPAC Name: 9-(4,6-dichloro-1,3,5-triazin-2-yl)carbazole
  • SMILES: C1=CC=C2C(=C1)C3=CC=CC=C3N2C4=NC(=NC(=N4)Cl)Cl
  • Synonyms: 24209-95-8, 9-(4,6-DICHLORO-1,3,5-TRIAZIN-2-YL)-9H-CARBAZOLE, DTXSID80731683, DTXCID60682427, 9-(4,6-dichloro-1,3,5-triazin-2-yl)carbazole

Application

This compound serves as a key intermediate in the synthesis of carbazole-based pharmaceuticals and optoelectronic materials. Its reactive dichlorotriazine group enables facile conjugation with nucleophiles, making it valuable for creating molecular scaffolds. Researchers utilize it in developing organic semiconductors and light-emitting materials due to the carbazole group’s electron-rich properties. The compound also finds use in polymer chemistry as a crosslinking agent or functional monomer.

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