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, category: thiazole
A series of 5-(N,N-disubstituted aminomethyl)-2-[(4- carbethoxymethylthiazol-2-yl)imino]-4-thiazolidinones 4a-m have been synthesized. Their structures are confirmed by elemental analyses and spectral data (IR, 1H NMR, EIMS). The antibacterial activities of the compounds against Staphylococcus aureus ATCC 6538, Staphylococcus epidermidis ATCC 12228, Escherichia coli ATCC 8739, Klebsiella pneumoniae ATCC 4352, Pseudomonas aeruginosa ATCC 1539, Salmonella typhi, Shigella flexneri, Proteus mirabilis ATCC 14153 and antifungal activity against Candida albicans ATCC 10231 are tested using disk diffusion method. Some of the compounds are found to have significant activity against S. aureus ATCC 6538.
A series of 5-(N,N-disubstituted aminomethyl)-2-[(4- carbethoxymethylthiazol-2-yl)imino]-4-thiazolidinones 4a-m have been synthesized. Their structures are confirmed by elemental analyses and spectral data (IR, 1H NMR, EIMS). The antibacterial activities of the compounds against Staphylococcus aureus ATCC 6538, Staphylococcus epidermidis ATCC 12228, Escherichia coli ATCC 8739, Klebsiella pneumoniae ATCC 4352, Pseudomonas aeruginosa ATCC 1539, Salmonella typhi, Shigella flexneri, Proteus mirabilis ATCC 14153 and antifungal activity against Candida albicans ATCC 10231 are tested using disk diffusion method. Some of the compounds are found to have significant activity against S. aureus ATCC 6538.
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.category: thiazole, you can also check out more blogs about53266-94-7
Reference£º
Thiazole | C3H10825NS – PubChem,
Thiazole | chemical compound | Britannica