Description

N-([1,1′-Biphenyl]-2-yl)-9,9-dimethyl-9H-fluoren-2-amine (CAS No. 1198395-24-2) is a high-purity organic compound with the molecular formula C₂₇H₂₃N. This advanced chemical features a fluorene core substituted with a dimethyl group at the 9-position and an amine-linked biphenyl moiety at the 2-position, offering unique steric and electronic properties. Ideal for materials science and pharmaceutical research, this compound is characterized by its robust stability and potential as a building block for optoelectronic materials, OLEDs, or ligand design. Supplied as a crystalline solid with ≥95% purity (HPLC), it is rigorously tested for consistency and performance. Store under inert conditions at -20°C to ensure long-term stability.

Properties

• CAS Number: 1198395-24-2
• Complexity: 518
• IUPAC Name: 9,9-dimethyl-N-(2-phenylphenyl)fluoren-2-amine
• InChI: InChI=1S/C27H23N/c1-27(2)24-14-8-6-13-22(24)23-17-16-20(18-25(23)27)28-26-15-9-7-12-21(26)19-10-4-3-5-11-19/h3-18,28H,1-2H3
• InChI Key: OBARUOOPPWHZRQ-UHFFFAOYSA-N
• Exact Mass: 361.183049738
• Molecular Formula: C27H23N
• Molecular Weight: 361.5
• SMILES: CC1(C2=CC=CC=C2C3=C1C=C(C=C3)NC4=CC=CC=C4C5=CC=CC=C5)C
• Topological: 12
• Monoisotopic Mass: 361.183049738
• Synonyms: 1198395-24-2, N-([1,1′-Biphenyl]-2-yl)-9,9-dimethyl-9H-fluoren-2-amine, N-[1,1′-Biphenyl]-2-yl-9,9-dimethyl-9H-fluoren-2-amine, 9,9-dimethyl-N-(2-phenylphenyl)fluoren-2-amine, 2-(2-Biphenylyl)amino-9,9-dimethylfluorene, 9H-Fluoren-2-amine, N-[1,1′-biphenyl]-2-yl-9,9-dimethyl-, MFCD19440968, N-[1,1/’-Biphenyl]-2-yl-9,9-dimethyl-9H-fluoren-2-amine, N-(2-Biphenylyl)-9,9-dimethyl-9H-fluoren-2-amine, SCHEMBL796162, DTXSID60735801, OBARUOOPPWHZRQ-UHFFFAOYSA-N, AKOS022175000, DS-7521, SY116413, DB-371251, B5122, CS-0135840, N-(2-Biphenyl)-9,9-dimethylfluorene-2-amine, N-(2-Biphenylyl)-9,9-dimethylfluoren-2-amine, biphenyl-2-yl-(9,9-dimethyl-9H-fluoren-2-yl)amine, N-(BIPHENYL-2-YL)-9,9-DIMETHYL-9H-FLUOREN-2-AMINE, N-[1,1 inverted exclamation marka-Biphenyl]-2-yl-9,9-dimethyl-9H-fluoren-3-amine

Application

N-([1,1′-Biphenyl]-2-yl)-9,9-dimethyl-9H-fluoren-2-amine is primarily used in the development of organic semiconductors and light-emitting materials due to its conjugated structure and electron-donating amine group. Researchers leverage its rigid biphenyl-fluorene hybrid scaffold to design thermally stable hole-transport layers (HTLs) for OLED devices. It also serves as a key intermediate in pharmaceutical synthesis for probing receptor-binding interactions. Its steric hindrance from the dimethylfluorene group makes it valuable in catalysis and ligand design.

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