Application of 453-20-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.453-20-3, Name is 3-Hydroxytetrahydrofuran, molecular formula is C4H8O2. In a Review，once mentioned of 453-20-3
Ethers are generally less reactive than other functionalized compounds such as alcohols. Therefore, cleavage of one of the C-O bonds in an ether group is not common in organic synthesis, except in the case of very reactive ethers such as benzyl ethers, tert-butyl ethers, and epoxides. The presence of two C-O bonds in each ether group causes another problem for the utilization of ether transformations in organic syntheses: The conversion of unsymmetrical ethers can produce two different sets of products. However, the recent focus on biomass conversion has renewed interest in ether conversions, because biomassderived materials often contain ether groups. An example of this is lignin,[1] which is a complex polyether of propylbenzene units. Furan derivatives are also important biomass-derived compounds.[2,3] Biomass resources generally contain large amounts of oxygen atoms and many functional groups. Removal of ether oxygen is one of the main reactions in biomass conversion, and ether hydrogenolysis (Scheme 1) achieves this end.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 453-20-3
Reference：
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem