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Atomfair 9,9-Dimethyl-3-phenyl-9H-fluoren-2-amine C21H19N

Description 9,9-Dimethyl-3-phenyl-9H-fluoren-2-amine (CAS No. 2123620-82-4) is a high-purity organic compound with the molecular formula C21H19N. This fluorene-based amine derivative features a phenyl substituent at the 3-position and a dimethyl group at the 9-position, offering unique steric and electronic properties for advanced research applications. Its rigid, planar fluorene backbone combined with the reactive amine group makes it a valuable intermediate in organic synthesis, materials science, and pharmaceutical research. This compound is supplied as a crystalline solid with ??95% purity (HPLC), ensuring consistency for demanding experimental protocols. Store under inert atmosphere at 2-8??C to maintain stability.

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Description

Description

9,9-Dimethyl-3-phenyl-9H-fluoren-2-amine (CAS No. 2123620-82-4) is a high-purity organic compound with the molecular formula C21H19N. This fluorene-based amine derivative features a phenyl substituent at the 3-position and a dimethyl group at the 9-position, offering unique steric and electronic properties for advanced research applications. Its rigid, planar fluorene backbone combined with the reactive amine group makes it a valuable intermediate in organic synthesis, materials science, and pharmaceutical research. This compound is supplied as a crystalline solid with ??95% purity (HPLC), ensuring consistency for demanding experimental protocols. Store under inert atmosphere at 2-8??C to maintain stability.

  • CAS No: 2123620-82-4
  • Molecular Formula: C21H19N
  • Molecular Weight: 285.4
  • Exact Mass: 285.151749610
  • Monoisotopic Mass: 285.151749610
  • IUPAC Name: 9,9-dimethyl-3-phenylfluoren-2-amine
  • SMILES: CC1(C2=CC=CC=C2C3=C1C=C(C(=C3)C4=CC=CC=C4)N)C
  • Synonyms: 9,9-Dimethyl-3-phenyl-9H-fluoren-2-amine, 2123620-82-4, 9,9-Dimethyl-3-phenyl-9H-fluoren-2-ylamine, SCHEMBL15506386, 9,9-dimethyl-3-phenylfluoren-2-amine

Application

9,9-Dimethyl-3-phenyl-9H-fluoren-2-amine serves as a key building block in the synthesis of optoelectronic materials due to its conjugated aromatic system. Researchers utilize it to develop novel fluorescent dyes and organic semiconductors for OLED applications. The compound’s sterically hindered amine group also makes it suitable for catalytic ligand design in asymmetric synthesis.

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