CAS: 101959-37-9; Octacosyl (E)-Ferulate

该化合物是一种合成酯,产自frulic酸,结合长链八氯基醇和生物活性苯酚类.该化合物由于存在四氢氧-3-甲基苯基组,具有显著的抗氧化特性,该组具有自由基和抑制氧化降解的作用.它的亲脂八氯基环乙烷链增强了与水分基体的稳定性和兼容性,使其适合涂层,聚合物和脂基配方的应用.该化合物的双重功能-抗氧化活动和结构多用途-在物质科学和工业化学中具有价值,特别是在需要长期氧化性抗药的情况下.其合成和纯度对于专业应用的一贯性至关重要.

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上下游产品

3-methoxy-4-(tetrahydropyran-2-yloxy)benzaldehyde prop-2-enoic acid(E)-3-3-Methoxy-4-(tetrahydropyran-2-yloxy)phenylprop-2-enoic acid°Ctacosanyl acetoxyferulate

合成工艺路线路线简述

    📜3-甲氧基-4-[(四氢-2H-吡喃-2-基)氧基]苯甲醛置于哌啶,苯胺 盐酸,N,N'-二环己基碳二亚胺体系中,用 四氢呋喃,吡啶 用作溶剂,化学反应 16.0H,反应生成(E)-阿魏酸二十八酯
    参考文献:Alkyl Ferulates In Wound Healing Potato Tubers
    标题:Alkyl Ferulates In Wound Healing Potato Tubers
    摘要:Seven Ferulic Acid Esters Of 1-Alkanols Ranging In Carbon Length From C-16 To C28 Were Synthesized And An HPLC Protocol For Their Separation Developed. Extracts Prepared From Wound Healing Potato (Solanum Tuberosum) Tubers And Analysed By HPLC Indicated That Alkyl Ferulate Esters Begin To Accumulate 3-7 Days After Wound Treatment. Of The Nine Esters Identified By Eims,(Including Two Esters Of Odd Chain Length Alkanols) Hexadecyl And octadecyl Ferulates Were Predominant. Alkyl Ferulate Esters Were Restricted To The Wound Periderm.
    Doi:10.1016/0031-9422(92)83695-U

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    ✅ COA系统入驻 | 共享模式

    合成参考文献

    合成方法参考DOI号:10.1016/0031-9422(92)83695-U
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