CAS: 24720-64-7; 2-(Triphenylphosphoranylidene)Propanal

该化合物是一种有机化合物,其特征是附于对丙二烯二甲酰胺的磷酰胺组,该化合物通常呈现黄色至橙色,在标准条件下以其稳定性而闻名;该化合物具有与甲酰胺功能组和三联苯磷酰胺相连接的中央碳原子,有助于其独特的再活动性和特性;三苯磷酰胺的出现,增强了其参与各种化学反应的能力,特别是有机合成的能力,在有机合成中,该化合物可以作为试剂或催化剂;此外,该化合物由于其同质系统,可能会表现出有趣的光学特性,使其对材料科学和光化学感兴趣;其溶解性一般在有机溶剂中,应谨慎处理,因为有可能与核分裂物发生再活动.

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上下游产品

CAS号4736-60-1 乙基三苯基碘化膦 | CAS号109-94-4 甲酸乙酯 | CAS号82248-14-4 [2-(Dimethylami... | CAS号90601-11-9 Phosphonium, [2... | CAS号1530-32-1 乙基三苯基溴化膦 | CAS号90601-12-0 Phosphonium, [2... | CAS号4736-60-1 乙基三苯基碘化膦 | CAS号494-90-6 薄荷呋喃 | CAS号28467-88-1 2-methylhex-2-enal | CAS号14250-96-5 反-2-甲基-2-戊烯醛 | CAS号62054-49-3 3-甲酰-2-丁烯酸乙酯 | CAS号184246-38-6 (2E)-2-Methyl-3... | CAS号1089733-35-6 (2Z)-2-methyl-3... | CAS号84188-96-5 3-(1,3-dithian-... | CAS号95532-05-1 2-methyl-5-phen...

合成工艺路线路线简述

    📜<2-(Dimethylamino)Vinyliden>Triphenylphosphoran置于sodium Hydroxide,硫酸体系中,用 苯 用作溶剂,化学反应 0.5H,反应生成2-(三苯基正膦基)丙醛
    参考文献:Bestmann,Hans Juergen; Schmid,Guenter; Oechsner,Helmut,Chemische Berichte,1984,Vol. 117,# 4,P. 1561-1571
    标题:Bestmann,Hans Juergen; Schmid,Guenter; Oechsner,Helmut,Chemische Berichte,1984,Vol. 117,# 4,P. 1561-1571

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    专利信息


    专利号:JP-WO2009104605-A1
    优先权日:2008-02-18
    标题 :A novel synthetic intermediate of ascofuranone with various physiological activities and a new shortened total synthesis method using it

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Total Synthesis Of Rhizoxin D, A Potent Antimitotic Agent From The Fungus Rhizopus ChinensiS
    作者:James D. White,Paul R. Blakemore,Neal J. Green,E. Bryan Hauser,Mark A. Holoboski,Linda E. Keown,Christine S. Nylund Kolz,Barton W. Phillips |发布日期:2002.11.1
    摘要:Configuration At C5 Of 2 Through A Stereoselective Addition Of The Radical Derived From Dehalogenation Of 21 At The Beta Carbon Of The (Z)-Alpha,Beta-Unsaturated Ester. Aldehyde 29 Was Obtained From Phenylthioacetal 24 And Condensed With Phosphorane 30, Representing Subunit B, In A Wittig Reaction That Gave The (E,E)-Dienoate 31. This Ester Was Converted To Aldehyde 33 In Preparation For Coupling With

    合成参考文献


    摘要:Abell, A. D.; Edmonds, M. K., Science of Synthesis, (2009) 46, 35.
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