The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 29390-67-8, Name is Mono-(6-amino-6-deoxy)-¦Â-cyclodextrin, SMILES is O[C@@H]1[C@H]([C@@H]2O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O[C@H](O[C@H]4CO)[C@@H](O)[C@H](O)[C@H]4O[C@H](O[C@H]5CO)[C@@H](O)[C@H](O)[C@H]5O[C@H](O[C@H]6CO)[C@@H](O)[C@H](O)[C@H]6O[C@H](O[C@H]7CO)[C@@H](O)[C@H](O)[C@H]7O[C@@H](O[C@@H]8CN)[C@H](O)[C@@H](O)[C@@H]8O[C@H]1O[C@@H]2CO)O)O)O, in an article , author is Kancharla, Suman, once mentioned of 29390-67-8, Quality Control of Mono-(6-amino-6-deoxy)-¦Â-cyclodextrin.
SYNTHESIS AND ANTIMICROBIAL ACTIVITIES OF NOVEL 2-(BENZO[D][1,3]DIOXOL-5-YL)-6,7-DIMETHOXYLQUINAZOLIN-4(3H)-ONES
In view of generatingnew compounds for future drug development, we have synthesized some 2-(benzo[d][1,3]dioxol-5-yl)-6,7-dimethoxylquinazolin-4(3H)-one derivatives of 4,5-dimethoxy-2-nitrobenzamide (5), synthesized by the ortho-nitro acid 4 was converted to its acid chloride by using thionyl chloride, followed by treatment with ammonia (aq.) gave the substituted ortho-nitro benzanilide (5). 4,5-Dimethoxy-2-nitrobenzamide (5) react withbenzo(d)[1,3] dioxole-5-carbaldehyde (6a) in presence of SnCl2 center dot 2H(2)O in MeOH was heated to gave 2-(benzo[d][1,3]dioxol-5-yl)-6,7-dimethoxylquinazolin-4(3H)-ones (7a-k). All the synthesized compounds were fully characterized on the basis of their detailed spectral studies and were evaluated for their antimicrobial activities in two Gram-positive bacteria (Staphylococcus aureus, Bacillus subtillis) and two Gram-negative bacteria (Echerichia coli and Pseudomonas aeuroginosa) and two fungi (Aspergillusniger and Aspergillusfumigatus) strains using Cup plate method
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Reference:
1,3-Benzodioxole – Wikipedia,
,Dioxole | C3H4O2 – PubChem