The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.3364-80-5, Name is Thiazole-4-carboxaldehyde, molecular formula is C4H3NOS. In a Article，once mentioned of 3364-80-5, Safety of Thiazole-4-carboxaldehyde
Selective Functionalization of 2-Nitro-p-phenylenediamine : Part III – A New Route to 1-Arylbenzimidazole 5-carbamates, Including Cambendazole
Reaction of 3,4-diaminophenylcarbamic acid ethyl ester (2) with carboxymethyl dithiobenzoate (3) gives the thiobenzanilides (4a or 4b), which could be cyclized by acid to 2-phenylbenzimidazole-5-carbamic acid ethyl ester (5).The same product is obtained by the reaction of 2 with benzaldehyde and sulphur.Other aromatic aldehydes have been similarly reacted to give (9b-d).Cambendazole (9e) is obtained by the reaction of thiazole-4-aldehyde and sulphur with 3,4-diaminophenylcarbamic acid isopropyl ester (6e).
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 Thiazole-4-carboxaldehyde, you can also check out more blogs about3364-80-5
Reference：
Thiazole | C3H9303NS – PubChem,
Thiazole | chemical compound | Britannica