53135-86-7Relevant academic research and scientific papers
Butylated hydroxy benzylidene ring: an important moiety for antioxidant synergism of semicarbazones
Nath, Amit R.,Yehye, Wageeh A.,Johan, Mohd Rafie Bin
, p. 2101 - 2114 (2020/09/22)
Abstract: The compounds having two or more antioxidant functions in their structure exhibit antioxidant synergism that generally increase the antioxidant activity of these compounds. In this study, two series of semicarbazone (7a–j and 7a′–j′) bearing butylated ortho and para hydroxy benzylidene ring were prepared for the investigation of antioxidant synergism. This study found that intramolecular hydrogen bond can form in semicarbazones due to the inappropriate position of hydroxyl group on benzylidene ring, which adversely affects the antioxidant synergism. As consequence, butylated para hydroxyl benzylidene phenyl semicarbazone (7a) (IC50 12.27?μM) showed ~ 4.3 times and ~ 2.7 times better antioxidant activity than compounds 7a′ (IC50 53.30?μM) and BHT (IC50 32.63?μM), respectively, in DPPH assay. In addition, based on the solubility in trimethylolpropane trioleate (TMPTO) as synthetic base oil and obtained IC50 results, oxidation stability of synthesized compounds was also evaluated by two kinds of differential scanning calorimeter (DSC) test, namely temperature ramping DSC and programmed temperature DSC. Thermogravimetric analysis is also performed for the thermal stability assessment. TMPTO incorporated with 0.25 mass% of 7c and 7e were found better oxidative (around 2 times) and thermal resistance than BHT. This DSC results showed another important aspect of semicarbazones that proper modification of semicarbazones can be used in the synthetic lubricant oil as a potential antioxidant. Thus, the results of this study are promising which can be taken under consideration to design and prepare more efficient multipotent semicarbazones. Graphic abstract: [Figure not available: see fulltext.]
Acid Hydrazide: A Potential Reagent for the Synthesis of Semicarbazones
Nath, Amit R.,Yehye, Wageeh A.
, p. 4301 - 4312 (2018/11/23)
Complex semicarbazone derivatives were successfully synthesized from substituted semicarbazides in acidic ethanol upon heating in the presence of aldehyde. The reaction is functional group tolerant and chemoselective because no terminal hydrazine moiety i
SYNTHESIS OF SOME THIOMETHYL DERIVATIVES OF 2,6-DI-tert-BUTYLPHENOL AND THEIR ANTIOXIDANT CHARACTERISTICS
Bilalov, S. B.,Alieva, F. D.,Gasanov, B. R.
, p. 1355 - 1357 (2007/10/02)
The reactions of 3,5-di-tert-butyl-4-hydroxybenzyl-N-N-dimethylamine with various thiols leads to the formation of 3,5-di-tert-butyl-4-hydoxybenzyl alkyl (aryl) sulfides.By means of their electrochemical oxidation at a stationary graphite microelectrode in aqueous media over a wide range of pH it was established that the new sulfides have the same level of antiradical activity as ionole. 3,5-Ditert-butyl-4-hydroxybenzyl sulfide is the most easily oxidized.
