In 2019,Organic Letters included an article by Si, Xiaojia; Zhang, Lumin; Hashmi, A. Stephen K.. Recommanded Product: 402-43-7. The article was titled 《Benzaldehyde- and Nickel-Catalyzed Photoredox C(sp3)-H Alkylation/Arylation with Amides and Thioethers》. The information in the text is summarized as follows:
Herein a synergistic combination of a nickel catalyst and benzaldehyde for the use of amides and thioethers in C(sp3)-H alkylation and arylation reactions employing simple aryl or alkyl halides is reported. This method provides a simple and cheap strategy for the direct functionalization of amides and thioethers. Readily available starting materials, mild reaction conditions, a good functional-group tolerance, and a broad substrate scope make this methodol. attractive and practical for pharmaceutical and synthetic chem. The experimental part of the paper was very detailed, including the reaction process of 1-Bromo-4-(trifluoromethyl)benzene(cas: 402-43-7Recommanded Product: 402-43-7)
1-Bromo-4-(trifluoromethyl)benzene(cas: 402-43-7) belongs to organobromine compounds. A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. Organobromine compounds have fallen under increased scrutiny for their environmental impact. Recommanded Product: 402-43-7
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary