On the use of diarylmaleimide derivatives in biological contexts: An investigation of the photochromic properties in aqueous solution was written by Fleming, Cassandra;Remon, Patricia;Li, Shiming;Simeth, Nadja Anita;Koenig, Burkhard;Groetli, Morten;Andreasson, Joakim. And the article was included in Dyes and Pigments in 2017.Related Products of 1195-14-8 This article mentions the following:
A series of photochromic diarylmaleimide derivatives has been synthesized and studied with respect to the photochromic properties in aqueous solution The main rationale is to investigate if these compounds could be used as photoswitchable units in biol. contexts, motivated by the fact that the diarylmaleimide structural motif is identified in many pharmacophores. Thus, photoswitchable variants of this class of compounds could be very useful in the quest for photoactivatable drugs. The photoinduced cyclization reaction (colorization) is suppressed in solvents of high polarity, whereas the ring-opening reaction (decolorization) still occurs with high efficiency. The photochromically active anti-parallel conformer of the open form is more abundant in the asym. substituted derivatives, which in turn favors the formation of the closed isomeric form. The rates of the thermal isomerization reactions have also been assessed, together with the resistance toward thermal degradation Here it was observed that the maleimide derived compounds were not susceptible to the thermally driven reactions (hydrolysis and isomerization). In the experiment, the researchers used many compounds, for example, 2-Methylbenzo[b]thiophene (cas: 1195-14-8Related Products of 1195-14-8).
2-Methylbenzo[b]thiophene (cas: 1195-14-8) belongs to benzothiophene derivatives. Benzothiophene finds use in research as a starting material for the synthesis of larger, usually bioactive structures. It is also used in the manufacturing of dyes such as thioindigo.Related Products of 1195-14-8
Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem