CAS: 13620-82-1; 4-Allyl-1,2-Phenylene Diacetate

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    4-allylpyr°C atechol acetic anhydride 1,2-dimethoxy-4-(2-propenyl)benzene 2-allyloxyphenol 3-(3',4'-dihydroxyphenyl)-1-propanol 4-[3-(acetyloxy)propyl]-1,2-phenylene diacetate 4-propyl-1,2-phenyl diacetate 4-(2,3-dihydroxypropyl)-1,2-phenylene diacetate

    合成工艺路线路线简述

    • 合成目标产物 Allylpyrocatechol -3,4-Diacetate 主要起始原料 4-Allylpyrocatechol And Acetic Anhydride
    • (文献来源)合成步骤主要原料 4-Allylpyrocatechol 和 Acetic Anhydride
    📜黄樟素置于4-二甲氨基吡啶,三氟化硼乙醚体系中,用 1,4-二氧六环,二氯甲烷 用作溶剂,化学反应 26.0H,反应生成4-烯丙基邻苯二酚二乙酸盐
    参考文献:New Catechol Derivatives Of Safrole And Their Antiproliferative Activity Towards Breast Cancer Cells
    标题:New Catechol Derivatives Of Safrole And Their Antiproliferative Activity Towards Breast Cancer Cells
    摘要:从黄樟素合成了儿茶酚.制备了九种衍生物,并使用不同的人类细胞系对其抗增殖作用进行了评估.体外生长抑制试验是基于磺胺染料来量化细胞活力.在对两种乳腺癌细胞系(mcf-7 和 Mda-Mb-231)进行的测试中,4-烯丙基-1,2-苯二醇(3),4-4-[3-(乙酰氧基)丙基]-1,2-亚苯基二乙酸酯(6)和 4-[3-(乙酰氧基)丙基]-5-硝基-1,2-亚苯基二乙酸酯(10)等衍生物的细胞毒性高于母体化合物 2.其 Ic50 值分别为 40.2 +/-6.9 μm,5.9 +/-0.8 μm 和 33.8 +/-4.9 μm,对真皮人成纤维细胞(dhf 细胞)无毒性.
    Doi:10.3390/molecules16064632

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1007/s12010-011-9353-5
    摘要:Rao K, Chodisetti B, Gandi S, Mangamoori LN, Giri A. Direct and Indirect Organogenesis of Alpinia galanga and the Phytochemical Analysis. Applied Biochemistry and Biotechnology. 2011 Sep 03;165(5-6):1366–78. doi: 10.1007/s12010-011-9353-5.
    参考文献:10.1007/s11947-022-02797-1
    摘要:Ling JKU, Sam JH, Jeevanandam J, Chan YS, Nandong J. Thermal Degradation of Antioxidant Compounds: Effects of Parameters, Thermal Degradation Kinetics, and Formulation Strategies. Food Bioprocess Technol. 2022 Mar 30;15(9):1919–35. doi: 10.1007/s11947-022-02797-1.
    参考文献:10.1007/978-3-031-22075-3_9
    摘要:Dev S. Alpinia galanga. 2023. In: Prime Ayurvedic Plant Drugs.
    参考文献:10.1007/978-3-031-43199-9_26
    摘要:Widyowati R, Pratama RR, Sholikhah I, Jain SK. Herbal Medicine and Rheumatic Disorders Management and Prevention. 2024. In: Reference Series in Phytochemistry.
    参考文献:10.1007/s00044-024-03357-2
    摘要:Cheng Y, Chen P, Dlamini ZM, Li J, Dlamini BS, Chen Y, Chang C. α-Glucosidase inhibitory activities of aromatic compounds from the rhizomes of Alpinia galanga. Med Chem Res. 2024 Nov 23;34(2):466–75. doi: 10.1007/s00044-024-03357-2.
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