Lophine
Lophine is the organic compound with the formula (C6H5C)2N2HCC6H5. It is a derivative of imidazole wherein all three carbon atoms have phenyl groups as substituents. A white solid, this compound gave the first example of chemiluminescence when its basic solutions were exposed to air.[1] Its chemiluminescence continues to attract attention.[2]
| Names | |
|---|---|
| Other names
2,4,5-triphenylimidazole | |
| Identifiers | |
| ECHA InfoCard | 100.006.915 |
PubChem CID |
|
CompTox Dashboard (EPA) |
|
| Properties | |
| C21H16N2 | |
| Molar mass | 296.373 g·mol−1 |
| Appearance | white solid |
| Density | 1,0874 g/cm3 |
| Melting point | 275 °C (527 °F; 548 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Lophine is prepared by condensation of benzaldehyde, benzil, and ammonia.[3]
References
- Radziszewski, B. R. (1877). "Untersuchungen über Hydrobenzamid, Amarin und Lophin". Berichte der Deutschen Chemischen Gesellschaft. 10: 70–75. doi:10.1002/cber.18770100122.
- Nakashima, Kenichiro (2003). "Lophine derivatives as versatile analytical tools". Biomedical Chromatography. 17 (2–3): 83–95. doi:10.1002/bmc.226. PMID 12717796.
- Bandivadekar, Priyanka V.; Chaturbhuj, Ganesh U. (2024). "Catalyst-free one-pot synthesis of 2,4,5-tri- and 1,2,4,5-tetrasubstituted imidazoles". Journal of Heterocyclic Chemistry. 61 (3): 430–438. doi:10.1002/jhet.4771.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.