Reference of 288-14-2, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.288-14-2, Name is Isoxazole, molecular formula is C3H3NO. In a article£¬once mentioned of 288-14-2
Synthesis, crystal structure, docking and antifungal activity of a new pyrazole acylurea compound
The title compound N-((3,5-dimethylphenyl)carbamoyl)-1-methyl-3-(trifluorome-thyl)-1H-pyrazole-4-carboxamide (C15H15F3N4O2) was synthesized, and its structure was confirmed by 1H NMR, H RMS and X-ray diffraction. It crystallizes in the triclinic system, space group P1 with a = 11.7147(5), b = 11.7935(5), c = 13.6620(5) A, alpha = 69.755(7), beta = 66.182(6), gamma = 72.100(7), Dc = 1.423 g/cm3, Z = 4, V = 1588.88(11) A3, the final R = 0.0347 and wR = 0.1005 for 7171 observed reflections with I > 2sigma(I). The preliminary biological test showed that the title compound has antifungal activities against Fusarium oxysporum, Pseudomonas syringae, Corynespora mazei and Botrytis cinerea at 100 mug/mL as 5.19%, 53.50%, 88.55% and 70.62%, respectively. The docking results indicated the hydrogen bonds formed between the compound and SHD.
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Reference£º
Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem