The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.38585-74-9, Name is Thiazol-5-ylmethanol, molecular formula is C4H5NOS. In a Article，once mentioned of 38585-74-9, Safety of Thiazol-5-ylmethanol
With the help of Surflex-Dock calculation, two ritonavir analogs in which one thioazole unit was replaced by selenazole have been designed and synthesized. The key selenazole structure was constructed from beta-azido diselenide through a cascade diselenide cleavage/selenocarbonylation/Staudinger reduction/aza-Wittig reaction and a following MnO2 oxidation. The accordingly prepared compounds exhibited good anti-HIV-1 (IIIB) activities comparable to that of the original ritonavir, as well as the positive SI values.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Safety of Thiazol-5-ylmethanol, you can also check out more blogs about38585-74-9
Reference：
Thiazole | C3H9141NS – PubChem,
Thiazole | chemical compound | Britannica