Extended knowledge of 63675-74-1

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application In Synthesis of 6-Methoxy-2-(4-methoxyphenyl)-1-benzothiophene, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 63675-74-1, in my other articles.

Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction by binding to a specific portion of an enzyme and thus slowing or preventing a reaction from occurring.Application In Synthesis of 6-Methoxy-2-(4-methoxyphenyl)-1-benzothiophene, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 63675-74-1, Name is 6-Methoxy-2-(4-methoxyphenyl)-1-benzothiophene, molecular formula is C16H14O2S

Anti-mitotic agents which inhibit tubulin polymerization

Methoxy and ethoxy substituted 3-aroyl-2-arylbenzo?b!thiophenes and benzo?b!thiophene analogues are described for use in inhibiting tubulin polymerization. The compounds’ use for treating tumor cells is also described.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application In Synthesis of 6-Methoxy-2-(4-methoxyphenyl)-1-benzothiophene, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 63675-74-1, in my other articles.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem