Description
N-([1,1′-Biphenyl]-3-yl)-4-methyl-[1,1′-biphenyl]-3-amine (CAS No. 1890112-83-0) is a high-purity organic compound with the molecular formula C25H21N. This biphenyl-based amine derivative features a methyl-substituted aromatic core, making it a valuable intermediate for advanced organic synthesis and materials science applications. Its IUPAC name, 2-methyl-5-phenyl-N-(3-phenylphenyl)aniline, reflects its precise structural configuration. The compound is supplied as a solid with confirmed identity via NMR and LC-MS analysis, ensuring reliability for research and industrial use. Ideal for use in OLEDs, pharmaceuticals, and ligand development, this product is handled under strict quality control to guarantee consistency and performance.
Properties
- CAS Number: 1890112-83-0
- Complexity: 406
- IUPAC Name: 2-methyl-5-phenyl-N-(3-phenylphenyl)aniline
- InChI: InChI=1S/C25H21N/c1-19-15-16-23(21-11-6-3-7-12-21)18-25(19)26-24-14-8-13-22(17-24)20-9-4-2-5-10-20/h2-18,26H,1H3
- InChI Key: NZQBCKJKAPGHOR-UHFFFAOYSA-N
- Exact Mass: 335.167399674
- Molecular Formula: C25H21N
- Molecular Weight: 335.4
- SMILES: CC1=C(C=C(C=C1)C2=CC=CC=C2)NC3=CC=CC(=C3)C4=CC=CC=C4
- Topological: 12
- Monoisotopic Mass: 335.167399674
- Synonyms: 1890112-83-0, N-([1,1′-Biphenyl]-3-yl)-4-methyl-[1,1′-biphenyl]-3-amine, SCHEMBL18762335
Application
This compound serves as a key building block in the synthesis of organic semiconductors and optoelectronic materials, particularly in OLED device fabrication. Its biphenyl-amine structure makes it suitable for use as a hole-transporting material in light-emitting diodes. Researchers also explore its potential in pharmaceutical intermediates and as a ligand in catalytic systems. The methyl substitution enhances solubility and processability in thin-film applications.
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