CAS: 42472-69-5; 1-(4-Ethynylphenyl)Ethanone

该化合物是一种有机化合物,其特点是其基酮功能组和苯环上的苯乙烯替代物,其特点是一种有机化合物,其分子结构包括一个附属于乙酰组的苯基组,其乙酰组(碳-碳三联联)相对于乙酰组处于准位置;该化合物一般没有色素,可变成黄色的液体或固体,视其纯度和温度而定;该化合物在有机合成中的应用情况而著称,特别是在生产各种药品和精细化学品方面;该苯乙烯组的存在增强了其再活动性,使其在有机化学的组合反应和其他变异方面有所助益;此外,该化合物还可能展示出有趣的光物理特性,可在材料科学和光化学中加以利用;与许多有机化合物一样,在处理时应采取安全防范措施,因为如果吸入或吸入,可能会对健康构成风险.

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上下游产品

4-(3-hydroxyprop-1-ynyl)acetophenone 4'-(2-trimethylsilylethynyl)acetophenone 1-(4-acetylphenyl)-3-methyl-1-butyn-3-ol 4-Iodoacetophenone 1-chloro-2-(4-acetylphenyl)ethyne 4-(phenylethinyl)acetophenone (E)-1-(4-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)phenyl)ethanone furan2-(p-acetylphenyl)benzofuran 3,5-dihydroxyphenol 2,4-diacetylphloroglucinol 1,3,5-triacetyl-2,4,6-trihydroxybenzene acetyl chloride 1-[2,4,6-tris-(4-nitro-benzoyloxy)-phenyl]-ethanone 2',4',6'-trihydroxy-3'-(3-methyl-2-butenyl)acetophenone 1-[2-hydroxy-3-(3-methyl-but-2-enyl)-4,6-bis-(3-methyl-but-2-enyloxy)-phenyl]-ethanone 1-[2,4,6-trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone

合成工艺路线路线简述

    📜1,1,2,2,3,3,4,4,4-Nonafluoro-Butane-1-Sulfonic Acid 4-Acetyl-Phenyl Ester置于bis-Triphenylphosphine-Palladium(II) Chloride Polymethylhydrosiloxane,18-冠醚-6,Potassium Carbonate,Cesium Fluoride,Copper(L) Chloride体系中,用 N-甲基吡咯烷酮,甲苯 作为反应溶剂,化学反应 13.0H,反应生成 4-乙炔基苯乙酮
    参考文献:Pmhs介导的炔烃或苯并噻唑与各种亲电试剂的偶联:在合成(-)-可可内酯a中的应用.
    标题:Pmhs介导的炔烃或苯并噻唑与各种亲电试剂的偶联:在合成(-)-可可内酯a中的应用.
    摘要:聚甲基氢硅氧烷(pmhs)与csf的结合有助于炔烃或苯并噻唑与一系列乙烯基,苯乙烯基和芳基卤化物或壬二酸酯以及酰基氯的交叉偶联.实验和光谱证据表明,这些反应涉及甲硅烷氧基中间体的原位反应生成.这些交叉偶联在室温和无胺条件下进行得相对较快.为了证明该方法的适用性,进行了全细胞毒性丁醇内酯(-)-可可内酯a的合成.
    DOI:10.1021/jo034463+

    海关参考信息

    专利信息


    专利号:US-7473797-B2
    优先权日:2004-04-27
    标 题 :Methods of 1,3-enyne preparation using copper (I) catalysts
    发明人:VENKATARAMAN DHANDAPANI; BATES CRAIG G; SAEJUENG PRANORM
    权利人:UNIV MASSACHUSETTS
    摘要:A copper(I) bi-dentate ligand complex-catalyzed procedure for synthesis of 1,3-enynes. The methods and/or systems of this invention afford a variety of enynes, tolerate a variety of sensitive functional groups, and can be employed without resort to expensive palladium reagents.

    专利号:US-11247905-B2
    优先权日:2016-11-18
    标题:Synthesis of graphene nanoribbons from monomeric molecular precursors bearing reactive alkyne moieties
    发明人:RUBIN YVES; JORDAN ROBERT S; LI YOLANDA L; MCCURDY RYAN D; KERVYN DE MEERENDRÉ SIMON
    权利人:UNIV CALIFORNIA
    摘要:A method of forming a graphene nanoribbon includes: 1) providing monomeric precursors each including an alkyne moiety and at least one aromatic moiety bonded to the alkyne moiety; 2) polymerizing the monomeric precursors to form a polymer; and 3) converting the polymer to a graphene nanoribbon.

    专利号:CN-114874141-A
    优先权日:2022-06-02
    标题:Synthesis of phenanthrene compounds by ring-opening cyclization of alkenyl benzotriazole under visible light catalysis

    专利号:US-7473786-B1
    优先权日:2003-12-05
    标题:Methods and systems for preparing fused heterocyclic compounds using copper(I) catalysts
    发明人:VENKATARAMAN DHANDAPANI; BATES CRAIG G; SAEJUENG PRANORM
    权利人:UNIV MASSACHUSETTS
    摘要:A copper(I)-catalyzed procedure for the synthesis of benzo[b]heterocycles. This protocol can be used to synthesize a variety of 2-arylbenzo[b]furans and indoles in good to excellent yields. This method can tolerate a variety of functional groups, does not require the use of expensive additives and is palladium-free.

    专利号:US-2020055735-A1
    优先权日:2016-11-18
    标题 :Synthesis of graphene nanoribbons from monomeric molecular precursors bearing reactive alkyne moieties

    专利号:CN-108395424-A
    优先权日:2018-02-08
    标 题:A method for the synthesis of benzothiophene derivatives from copper-catalyzed dihalogenated arenes under microwave radiation

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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

    主要参考文献

    参考标题:Rhodium( Ii )‐catalyzed [4+3] Cyclization Of Triazoles With Indole Derivatives And Its Application In The Total Synthesis Of (+/-)‐aurantioclavine
    作者:Shengguo Duan,Bing Xue,Hui Meng,Zihang Ye,Ze‐feng Xu,Chuan‐ying Li |发布日期:2021.5
    摘要:Rhodium(II)‐catalyzed [4+3] Cyclization Reaction Of 1‐sulfonyl‐1,2‐3‐triazoles And Indoles Was Developed. Azepino[5,4,3‐ Cd]Indoles, Which Are Widely Distributed In Ergot Alkaloids With Various Biological Activities, Could Be Obtained In Good To Excellent Yields. In Addition, The Total Synthesis Of (+/-)‐aurantioclavine Was Completed In Four Steps From The Known Compound 1A Adopting This [4+3] Cyclization As A Key Step

    合成参考文献


    摘要:Ferris, G. E.; Mlynarski, S. N.; Morken, J. P., Science of Synthesis Knowledge Updates, (2012) 3, 234.
    摘要:Krause, N.; Arisetti, N., Science of Synthesis Knowledge Updates, (2020) 3, 104.
    摘要:Trofimova, A.; Sirvinskas, M.; Yudin, A. K., Science of Synthesis Knowledge Updates, (2021) 2, 73.
    摘要:Anderson, E. A.; Lim, D. S. W., Science of Synthesis Knowledge Updates, (2015) 1, 75.
    摘要:Kwiecień, H., Science of Synthesis Knowledge Updates, (2014) 4, 63.
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