A sun-screening agent isooctyl p-methoxy cinnamate was prepared by reaction of p-methoxyl benzaldehyde with isooctyl acetate using titanium tetrachloride as catalyst. The optimum conditions are as follows: molar rati...A sun-screening agent isooctyl p-methoxy cinnamate was prepared by reaction of p-methoxyl benzaldehyde with isooctyl acetate using titanium tetrachloride as catalyst. The optimum conditions are as follows: molar ratio of p-methoxyl benzaldehyde to isooctyl acetate and titanium tetrachloride is 1 : 1.1 : 0.5; reaction temperature is 30℃; and reaction time is 6 h. The yield of isooctyl p-methoxy cinnamate can reach 98%. The method of the synthesis of isooctyl p-methoxy cinnamate is efficient and economical.展开更多
A new series of azo were derived from 2,5-di(p-amino phenyl)-3,6-diphenyl pyrazine in the presence of benzoic acid, salicylic acid, p-amino salicylic acid, p-methoxy phenol and pmethyl phenol. The structures of the ...A new series of azo were derived from 2,5-di(p-amino phenyl)-3,6-diphenyl pyrazine in the presence of benzoic acid, salicylic acid, p-amino salicylic acid, p-methoxy phenol and pmethyl phenol. The structures of the synthesized compounds were determined on the basis of their FTIR, UV (ultraviolet), elemental analysis and H-NMR (H-nuclear magnetic resonance) spectral date. The purity of synthesized compounds was checked by performing TLC (thin layer chromatography). The antibacterial activity was evaluated in DMSO (dimethyl sulfoxide).展开更多
文摘A sun-screening agent isooctyl p-methoxy cinnamate was prepared by reaction of p-methoxyl benzaldehyde with isooctyl acetate using titanium tetrachloride as catalyst. The optimum conditions are as follows: molar ratio of p-methoxyl benzaldehyde to isooctyl acetate and titanium tetrachloride is 1 : 1.1 : 0.5; reaction temperature is 30℃; and reaction time is 6 h. The yield of isooctyl p-methoxy cinnamate can reach 98%. The method of the synthesis of isooctyl p-methoxy cinnamate is efficient and economical.
文摘A new series of azo were derived from 2,5-di(p-amino phenyl)-3,6-diphenyl pyrazine in the presence of benzoic acid, salicylic acid, p-amino salicylic acid, p-methoxy phenol and pmethyl phenol. The structures of the synthesized compounds were determined on the basis of their FTIR, UV (ultraviolet), elemental analysis and H-NMR (H-nuclear magnetic resonance) spectral date. The purity of synthesized compounds was checked by performing TLC (thin layer chromatography). The antibacterial activity was evaluated in DMSO (dimethyl sulfoxide).