CAS: 159853-36-8; 4'-O-Methylirenolone

该化合物是有机化合物,其特点是复杂的多环结构,包括一个苯乙烯核心,具有有机化合物特征,该化合物具有氢氧基(-OH)和与芳香环相连的甲基氧基(-OCH3),有助于其化学反应和潜在的生物活动.这些功能组的存在表明,该化合物可能具有诸如抗氧化活动或与生物目标可能发生相互作用等特性.该化合物由于其芳香性质,有可能溶于有机溶剂中,而其在水中的溶解性可能有限.其分子结构允许在有机合成,材料科学等领域以及可能存在于医药中的各种应用,取决于其生物活动.与许多有机化合物一样,在处理和使用时,应参考安全数据,因为其可能造成健康风险或环境关切.

结构式图片

上下游产品

3-(4-Methoxy-phenyl)-3b,4a-dihydro-4-oxa-cyclopropa[a]phenalen-5-one Perinaphthenon 9-(4-methoxyphenyl)-1H-phenalen-1-one 4-methoxyphenyl magnesium bromide irenolone

合成工艺路线路线简述

    📜萘嵌苯酮置于叔丁基过氧化氢,Jones Reagent,苄基三甲基氢氧化铵,二异丁基氢化铝,对甲苯磺酸,2,3-二氯-5,6-二氰基-1,4-苯醌体系中,用 二氯甲烷,苯 用作溶剂,化学反应 12.25H,反应生成2-羟基-4-(4-甲氧基苯基)-1H-萘嵌苯-1-酮
    参考文献:Phenalenone-Type Phytoalexins From Musa Acuminata Synthesis Of 4-Phenyl-Phenalenones
    标题:Phenalenone-Type Phytoalexins From Musa Acuminata Synthesis Of 4-Phenyl-Phenalenones
    摘要:Two New 4-Phenyl-Phenalenone-Type Phytoalexins (2,3) Have Been Isolated From Rhizomes Of Musa Acuminata Infected With The Fungus Fusarium Oxysporum. The Structures Of The New Phytoalexins Were Elucidated On The Basis Of Spectroscopic Evidence,Chemical Correlation And Synthesis From Commercial Phenalen-1-One. The Chemical Shift For All Of The Hydrogen And Carbon Atoms In The Substances Were Unambiguously Established By Mono-And Bidimensional,Homo-And Heteronuclear NMR Experiments (H-1 NMR,C-13 NMR Cosy,Hmqc And Hmbc). In Preliminary ''In Vitro'' Assays,The New Phytoalexins Have Shown Inhibitory Activity On The Growth Of The Germinative Tube Of Fusarium Oxysporum F. Sp. Cubense Race 4.
    Doi:10.1016/s0040-4020(01)85707-0

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    📌 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:10.1016/s0040-4020(97)00490-0
    摘要:Luis JG, Lahlou EH, Andrés LS, Echeverri F, Fletcher WQ. Phenylphenalenonic phytoanticipins. New acenaphtylene and dimeric phenylphenalenones from the resistant Musa selected hybrid SH-3481. Tetrahedron. 1997 Jun;53(24):8249–56. doi: 10.1016/s0040-4020(97)00490-0.
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