CAS: 6750-60-3; (1Ar,4Ar,7S,7Ar,7Br)-1,1,7-Trimethyl-4-Methylenedecahydro-1H-Cyclopropa[e]Azulen-7-Ol

该化合物是一种自然产生的松树醇,主要存在于各种基本油类中,特别是来自阿斯特拉夏家族植物的植物,其特点是复杂的双环结构,有助于其独特的化学特性. 甲状腺素以其令人愉快的,土味的芳香闻名而闻名,使它成为香味和口味产业中的宝贵成分. 化合物展示了一系列生物活动,包括抗微生物,抗炎和潜在的抗癌特性,它们引起了药理研究的兴趣. 其分子式为C15H24O, 其特征为可增加极地溶剂溶性的一个氢氧基组. 甲状腺素通常通过蒸汽蒸馏或溶剂提炼方法与植物来源隔绝. 由于其多种用途和潜在的健康利益,它继续成为天然产品化学和药学研究的研究对象.

结构式图片

上下游产品

(+)-11β-hydroxy-apoaromadendrone Methylenetriphenylphosphorane Chloromethyltrimethylsilane (1S,3aR,8aS)-3a-methyl-7-methylidene-1-propan-2-yl-2,3,5,6,8,8a-hexahydro-1H-azulen-4-oneβ-Spathulen 4β,10β-aromadendranediol 4β,10α-aromadendranediol

合成工艺路线路线简述

    📜Bicyclogermacrene置于间氯过氧苯甲酸体系中,用 氘代氯仿,氯仿 作为反应溶剂,化学反应 0.25H,以57%的收率获得产物桉油烯醇
    参考文献:通过平台萜烯(+)-Bicyclogermacrene仿生合成(+)-Ledene,(+)-Viridiflorol,(-)-Palustrol,(+)-Spathulenol以及psiguadial A,C和d
    标题:通过平台萜烯(+)-Bicyclogermacrene仿生合成(+)-Ledene,(+)-Viridiflorol,(-)-Palustrol,(+)-Spathulenol以及psiguadial A,C和d
    摘要:(+)-Bicyclogermacrene是在几种精油中发现的一种紧张的双环和倍半萜烯.据报道,短短且高收率的双环锗烷的合成分七个步骤进行.该萜烯用作仿生进入几种芳香树烯倍半萜的关键平台中间体,如香豆素,Viridiflorol,Palestrol和spathulenol.此外,双环germacrene被证明是合成异丙基萜类化合物a,C和d中的萜烯成分.
    DOI:10.1002/chem.201403082

    海关参考信息

    专利信息


    专利号:US-9474270-B2
    优先权日:2001-05-08
    标 题 :Methods and compositions for controlling pests
    发明人:SPOONER-HART ROBERT NEIL; BASTA ALBERT HABIB
    权利人:BIO-GENE TECH LTD; BIOPROSEPECT LTD; UNIV OF WESTERN SYDNEY
    摘要:The present invention is directed to pest-controlling compositions comprising as active ingredients one or more β-diones, particularly β-diketones and β-triketones, and to the use of these compositions inter alia for preventing, eradicating, destroying, repelling or mitigating harmful, annoying or undesired pests including insects, arachnids, helminths, molluscs, protozoa and viruses. The present invention is further directed to processes of preparing β-diones by de novo synthesis or from natural sources such as volatile oil-bearing plants from families including Alliaceae, Apiaceae, Asteraceae, Cannabinaceae, Lamiaceae, Pteridaceae, Myrtaceae, Myoporaceae, Proteaceae, Rutaceae and Zingiberaceae.

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1515/znc-2009-11-1214
    摘要:Pérez-Hernández N, Ponce-Monter H, Ortiz MI, Cariño-Cortés R, Joseph-Nathan P. Structure-activity relationships of aromadendranes in uterus-relaxant activity. Z Naturforsch C J Biosci. 2009 Nov;64(11-12):840–6. doi: 10.1515/znc-2009-11-1214.
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