Anderson, M. R.; Andringa, S.; Anselmo, L.; Arushanova, E.; Asahi, S.; Askins, M.; Auty, D. J.; Back, A. R.; Barnard, Z.; Barros, N.; Bartlett, D.; Barao, F.; Bayes, R.; Beier, E. W.; Bialek, A.; Biller, S. D.; Blucher, E.; Bonventre, R.; Boulay, M.; Braid, D.; Caden, E.; Callaghan, E. J.; Caravaca, J.; Carvalho, J.; Cavalli, L.; Chauhan, D.; Chen, M.; Chkvorets, O.; Clark, K. J.; Cleveland, B.; Cookman, D.; Connors, C.; Coulter, I. T.; Cox, M. A.; Cressy, D.; Dai, X.; Darrach, C.; Davis-Purcell, B.; Deluce, C.; Depatie, M. M.; Descamps, F.; Dittmer, J.; Lodovico, F. Di; Duhaime, N.; Duncan, F.; Dunger, J.; Earle, A. D.; Fabris, D.; Falk, E.; Farrugia, A.; Fatemighomi, N.; Fischer, V.; Fletcher, E.; Ford, R.; Frankiewicz, K.; Gagnon, N.; Gaur, A.; Gilje, K.; Gonzalez-Reina, O. I.; Gooding, D.; Gorel, P.; Graham, K.; Grant, C.; Grove, J.; Grullon, S.; Guillian, E.; Hall, S.; Hallin, A. L.; Hallman, D.; Hans, S.; Hartnell, J.; Harvey, P.; Hedayatipour, M.; Heintzelman, W. J.; Heise, J.; Helmer, R. L.; Horne, D.; Hreljac, B.; Hu, J.; Hussain, A. S. M.; Iida, T.; Inacio, A. S.; Jackson, C. M.; Jelley, N. A.; Jillings, C. J.; Jones, C.; Jones, P. G.; Kamdin, K.; Kaptanoglu, T.; Kaspar, J.; Keeter, K.; Kefelian, C.; Khaghani, P.; Kippenbrock, L.; Klein, J. R.; Knapik, R.; Kofron, J.; Kormos, L. L.; Korte, S.; Krar, B.; Kraus, C.; Krauss, C. B.; Kroupova, T.; Labe, K.; Lafleur, F.; Lam, I.; Lan, C.; Land, B. J.; Lane, R.; Langrock, S.; LaTorre, A.; Lawson, I.; Lebanowski, L.; Lefeuvre, G. M.; Leming, E. J.; Li, A.; Lidgard, J.; Liggins, B.; Lin, Y. H.; Liu, X.; Liu, Y.; Lozza, V.; Luo, M.; Maguire, S.; Maio, A.; Majumdar, K.; Manecki, S.; Maneira, J.; Martin, R. D.; Marzec, E.; Mastbaum, A.; Mauel, J.; McCauley, N.; McDonald, A. B.; Mekarski, P.; Meyer, M.; Miller, C.; Mills, C.; Mlejnek, M.; Mony, E.; Morton-Blake, I.; Mottram, M. J.; Nae, S.; Nirkko, M.; Nolan, L. J.; Novikov, V. M.; O’Keeffe, H. M.; O’Sullivan, E.; Gann, G. D. Orebi; Parnell, M. J.; Paton, J.; Peeters, S. J. M.; Pershing, T.; Petriw, Z.; Petzoldt, J.; Pickard, L.; Pracsovics, D.; Prior, G.; Prouty, J. C.; Quirk, S.; Reichold, A.; Riccetto, S.; Richardson, R.; Rigan, M.; Robertson, A.; Rose, J.; Rosero, R.; Rost, P. M.; Rumleskie, J.; Schumaker, M. A.; Schwendener, M. H.; Scislowski, D.; Secrest, J.; Seddighin, M.; Segui, L.; Seibert, S.; Semenec, I.; Shaker, F.; Shantz, T.; Sharma, M. K.; Shokair, T. M.; Sibley, L.; Sinclair, J. R.; Singh, K.; Skensved, P.; SMILESy, M.; Sonley, T.; Stainforth, R.; Strait, M.; Stringer, M. I.; Svoboda, R.; Sorensen, A.; Tam, B.; Tatar, J.; Tian, L.; Tolich, N.; Tseng, J.; Tseung, H. W. C.; Turner, E.; Van Berg, R.; Veinot, J. G. C.; Virtue, C. J.; von Krosigk, B.; Vazquez-Jauregui, E.; Walker, J. M. G.; Walker, M.; Walton, S. C.; Wang, J.; Ward, M.; Wasalski, O.; Waterfield, J.; Weigand, J. J.; White, R. F.; Wilson, J. R.; Winchester, T. J.; Woosaree, P.; Wright, A.; Yanez, J. P.; Yeh, M.; Zhang, T.; Zhang, Y.; Zhao, T.; Zuber, K.; Zummo, A.; SNO& Collaboration published an article about the compound: 2,5-Diphenyloxazole( cas:92-71-7,SMILESS:C1(C2=CC=CC=C2)=NC=C(C3=CC=CC=C3)O1 ).Electric Literature of C15H11NO. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:92-71-7) through the article.
A liquid scintillator consisting of linear alkylbenzene as the solvent and 2,5-diphenyloxazole as the fluor was developed for the SNO+ experiment This mixture was chosen as it is compatible with acrylic and has a competitive light yield to pre-existing liquid scintillators while conferring other advantages including longer attenuation lengths, superior safety characteristics, chem. simplicity, ease of handling, and logistical availability. Its properties have been extensively characterized and are presented here. This liquid scintillator is now used in several neutrino physics experiments in addition to SNO+.
There is still a lot of research devoted to this compound(SMILES：C1(C2=CC=CC=C2)=NC=C(C3=CC=CC=C3)O1)Electric Literature of C15H11NO, and with the development of science, more effects of this compound(92-71-7) can be discovered.
Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica