Mn-Catalyzed Electrochemical Synthesis of Quinazolinones from Primary Alcohols/Benzyl Ethers and o-Aminobenzamides was written by Lin, Dian-Zhao;Lai, Yin-Long;Huang, Jing-Mei. And the article was included in ChemElectroChem in 2019.SDS of cas: 119023-25-5 This article mentions the following:
An efficient approach for the synthesis of quinazolinones I [R1 = n-Bu, Ph, 3-pyridyl, etc.; R2 = 4-Me, 3-OMe, 3-Br, etc; R3 = H, Me] from o-aminobenzamides and primary alcs./benzyl ethers using combination of electrochem. and redox-metal catalysis was developed. Taking manganese(II) sulfate as a redox catalyst, this transformation proceeded smoothly under ambient conditions in an undivided cell to afford I in moderate to excellent yields with a wide substrate scope. In the experiment, the researchers used many compounds, for example, 2-Amino-4-fluorobenzamide (cas: 119023-25-5SDS of cas: 119023-25-5).
2-Amino-4-fluorobenzamide (cas: 119023-25-5) belongs to amides. Amides include many other important biological compounds, as well as many drugs like paracetamol, penicillin and LSD. Low-molecular-weight amides, such as dimethylformamide, are common solvents. Amides are stable compounds. The lower-melting members (such as acetamide) can be readily purified by fractional distillation. Most amides are solids which have low solubilities in water.SDS of cas: 119023-25-5
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics