Application of 4265-25-2, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.4265-25-2, Name is 2-Methylbenzofuran, molecular formula is C9H8O. In a Review，once mentioned of 4265-25-2
Halide clusters of Group 5?7 metals develop catalytic activity above 150?250 C, and the activity is retained up to 350?450 C by taking advantage of their thermal stability, low vapor pressure, and high melting point. Two types of active site function: the solid Br°nsted acid site and a coordinatively unsaturated site that catalyzes like the platinum metals do. Various types of catalytic reactions including new reactions and concerted catalyses have been observed over the clusters: hydrogenation, dehydrogenation, hydrogenolysis, isomerization of alkene and alkyne, and alkylation of toluene, amine, phenol, and thiol. Ring-closure reactions to afford quinoline, benzofuran, indene, and heterocyclic common rings are also catalyzed. Beckmann rearrangement, S-acylation of thiol, and dehydrohalogenation are also catalyzed. Although the majority of the reactions proceed over conventional catalysts, closer inspection shows some conspicuous features, particularly in terms of selectivity. Halide cluster catalysts are characterized by some aspects: cluster counter anion is too large to abstract counter cation from the protonated reactants, cluster catalyst is not poisoned by halogen and sulfur atoms. Among others, cluster catalysts are stable at high temperatures up to 350?450 C. At high temperatures, apparent activation energy decreases, and hence weak acid can be a catalyst without decomposing reactants.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 4265-25-2, and how the biochemistry of the body works.Application of 4265-25-2
Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H219O – PubChem