One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Safety of Benzo[b]furan-2-carboxaldehyde, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 4265-16-1, Name is Benzo[b]furan-2-carboxaldehyde, molecular formula is C9H6O2
A brief synthesis of 2,2?-arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) catalyzed by TEAOH in various solvents
Aims and Objectives: 2,2?-Arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) having four carbonyl functionalities along with their tautomeric keto-enol forms, is an important biologically active compound and important synthetic intermediate in the synthesis of xanthenes. This study was conducted in order to develop a new and concise method of synthesis of 2,2?-arylmethylene bis (3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) derivatives. Materials and Methods: TEAOH (20 mol %) was fond to be as a simple and efficient catalyst for the preparation of 2,2?-arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) derivatives by the Knoevenagel condensation/Michael addition tandem reactions. Results: A concise and practical method was developed for one-pot synthesis of 2,2?-arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) derivatives catalyzed by TEAOH at room temperature in various solvents. Conclusion: This strategy provides several advantages over the traditional synthetic method, and is applicable to a wide variety of aromatic and heteroaromatic aldehydes at room temperature in various solvents.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Safety of Benzo[b]furan-2-carboxaldehyde, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 4265-16-1, in my other articles.
Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H825O – PubChem