Computed Properties of C11H16OIn 2020, Bub, Christina L.;Thoennissen, Vinzenz;Patureau, Frederic W. published 《Benzophenothiazine and Its Cr(III)-Catalyzed Cross Dehydrogenative Couplings》. 《Organic Letters》published the findings. The article contains the following contents:
In stark contrast to phenothiazines and their prevalence for cross-dehydrogenative amination reactions, benzophenothiazine has a pronounced preference for cross-dehydrogenative C-C bond-forming reactions. Moreover, the substrate is very versatile, leading to several new classes of C-C bond-forming reactions and many new oxidative coupling product architectures, including unprecedented indole fused paddlewheel-like structures. To complete the study, the researchers used 4-tert-Amylphenol (cas: 80-46-6) .
4-tert-acylphenol (cas:80-46-6) contains hydroxyl group. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble.Computed Properties of C11H16O
Reference:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts