| Identification | Back Directory | [Name]
1-(4-Aminophenyl)-1,2,2-triphenylethene | [CAS]
919789-80-3 | [Synonyms]
JACS-919789-80-3
4-(1,2,2-Triphenylvinyl)aniline
4-(1,2,2-triphenylethenyl)aniline
4-(1,2,2-triphenylethenyl)-benzenamine
1-(4-Aminophenyl)-1,2,2-triphenylethene
BENZENAMINE, 4-(1,2,2-TRIPHENYLETHENYL)-
1-(4-Aminophenyl)-1,2,2-triphenylethene ISO 9001：2015 REACH | [Molecular Formula]
C26H21N | [MDL Number]
MFCD31697689 | [MOL File]
919789-80-3.mol | [Molecular Weight]
347.45 |
| Chemical Properties | Back Directory | [Melting point ]
202.1-203.4 °C | [Boiling point ]
472.6±24.0 °C(Predicted) | [density ]
1.128±0.06 g/cm3(Predicted) | [pka]
4.16±0.10(Predicted) | [InChI]
InChI=1S/C26H21N/c27-24-18-16-23(17-19-24)26(22-14-8-3-9-15-22)25(20-10-4-1-5-11-20)21-12-6-2-7-13-21/h1-19H,27H2 | [InChIKey]
WCNQRPKNQRXHQJ-UHFFFAOYSA-N | [SMILES]
C1(N)=CC=C(/C(/C2=CC=CC=C2)=C(\C2=CC=CC=C2)/C2=CC=CC=C2)C=C1 |
| Questions And Answer | Back Directory | [Application]
1-(4-aminophenyl)-1,2,2-triphenylene can be used as a synthetic intermediate, such as in the preparation of tetraphenylethene (TPE) compounds. These compounds possess a large conjugated system, with the four benzene rings of the molecule linked to a single isolated double bond. Due to steric hindrance, the benzene rings twist relative to each other, resulting in a propeller-like molecule. Tetraphenylethene compounds exhibit excellent luminescent properties and are easily synthesized, making them superior aggregation-induced emission (AIE) compounds. They have been extensively studied in fields such as organic light-emitting diodes, liquid crystal devices, supramolecular assembly, drug release, and sensors. |
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