COA of Formula: C8H8O2. In 2021 CHEM HETEROCYCL COM+ published article about KNOEVENAGEL-MICHAEL REACTION; C-H ACIDS; MULTICOMPONENT REACTIONS; HETEROCYCLIC CHEMISTRY; CARBONYL-COMPOUNDS; 1ST EXAMPLE; EFFICIENT; CONVENIENT; FACILE; MALONONITRILE in [Elinson, Michail N.; Vereshchagin, Anatoly N.; Ryzhkova, Yuliya E.; Karpenko, Kirill A.; Ryzhkov, Fedor V.; Egorov, Mikhail P.] Russian Acad Sci, ND Zelinsky Inst Organ Chem, 47 Leninsky Ave, Moscow 119991, Russia in 2021, Cited 64. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.
Electrocatalytic transformation of aldehydes with two equivalents of 1,3-diethyl-2-thiobarbituric acid has been carried out in alcohols in an undivided cell in the presence of sodium halides with the selective formation of the substituted 5,5′-(arylmethylene)bis(1,3-diethyl-2-thiobarbituric acids) in 87-98% yields and with 870-980% current efficiency. This new one-pot electrochemically induced tandem Knoevenagel-Michael process is a simple and efficient approach to substituted 5,5′-(arylmethylene)bis(1,3-diethyl-2-thiobarbituric acids) containing two 1,3-diethyl-2-thiobarbituric acid fragments separated by C-aryl-substituted spacer, which are promising compounds for different biomedical applications, including anticonvulsant, antiAIDS agents and anti-inflammatory remedies. Theoretical studies were carried out to investigate the interaction of the synthesized compounds with beef and human catalases.
About 4-Methoxybenzaldehyde, If you have any questions, you can contact Elinson, MN; Vereshchagin, AN; Ryzhkova, YE; Karpenko, KA; Ryzhkov, FV; Egorov, MP or concate me.. COA of Formula: C8H8O2
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles