In 2019,Chemical Communications (Cambridge, United Kingdom) included an article by Chen, Jian; Zhu, Shengqing; Qin, Jian; Chu, Lingling. Recommanded Product: 100-48-1. The article was titled 《Intermolecular, redox-neutral azidoarylation of alkenes via photoredox catalysis》. The information in the text is summarized as follows:
An intermol., redox-neutral azidoarylation of alkenes with pyridines and TMSN3 was reported via visible light-induced photoredox catalysis. This protocol utilized a radical addition/radical coupling sequence, allowing for facile and regioselective installation of versatile β-azido pyridines under redox-neutral and mild conditions. In the experiment, the researchers used 4-Cyanopyridine(cas: 100-48-1Recommanded Product: 100-48-1)
4-Cyanopyridine(cas: 100-48-1) belongs to pyridine. Pyridine’s structure is isoelectronic with that of benzene, but its properties are quite different. Pyridine is completely miscible with water, whereas benzene is only slightly soluble. Like all hydrocarbons, benzene is neutral (in the acid–base sense), but because of its nitrogen atom, pyridine is a weak base.Recommanded Product: 100-48-1