The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.53266-94-7, Name is Ethyl 2-(2-aminothiazol-4-yl)acetate, molecular formula is C7H10N2O2S. In a Article，once mentioned of 53266-94-7, SDS of cas: 53266-94-7
The conformations and hydrogen bonding in the thiophene and thiazole title compounds, [Fe(C5H5)(C20H14NO 3S)], (I), and [Fe(C5H5)(C19H 17N2O3S)], (II), are discussed. The sequence (C5H4)-(C6H4)-(CONH)-(C 4H2S)-(CO2Me) of rings and moieties in (I) is close to being planar; all consecutive interplanar angles are less than 10. An intramolecular N-H…O=Cester hydrogen bond [graph set S(6), N…O = 2.768 (2) A and N – H…O = 134 (2)] effects the molecular planarity, and aggregation occurs via hydrogen-bonded chains formed from intermolecular Car – H…O=Cester/amide interactions along [010], with C…O distances ranging from 3.401 (3) to 3.577 (2) A. The thiazole system in (II) crystallizes with two molecules in the asymmetric unit; these differ in the conformation along their long molecular axes; for example, the interplanar angle between the phenylene (C 6H4) and thiazole (C3NS) rings is 8.1 (2) in one molecule and 27.66 (14) in the other. Intermolecular N-H…O=Cester hydrogen bonds [N…O = 2.972 (4) and 2.971 (3) A], each augmented by a Cphenylene – H…O=C ester interaction [3.184 (5) and 3.395 (4) A], form motifs with graph set R21(7) and generate chains along [100]. The amide C=O groups do not participate in hydrogen bonding. Compound (II) is the first reported ferrocenyl-containing thiazole structure.
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.SDS of cas: 53266-94-7, you can also check out more blogs about53266-94-7
Reference：
Thiazole | C3H10736NS – PubChem,
Thiazole | chemical compound | Britannica