CAS: 719-80-2; Ethoxydiphenylphosphine

该化合物是一种有机磷的化合物,其特点是存在磷化物功能组,该化合物一般看起来是无色的,不光彩的黄色液体,在正常条件下因其稳定性而闻名.乙酰P,P-二苯基硫酸盐具有与磷原子相连的两个苯基组的特点,有助于其独特的化学特性,包括其在化学协调中作为离子体作用的能力.该化合物经常用于有机合成和作为各种化学反应的试剂,特别是在形成氧化磷和其他含磷的化合物时.该化合物具有中度毒性,需要适当的处理安全措施.其在有机溶剂中的溶解性使其在不同的化学环境中具有多种用途.

结构式图片

欧盟法规

REACH注册ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

CAS号1079-66-9 氯代二苯基膦 | CAS号64-17-5 乙醇 | CAS号100-58-3 苯基溴化镁 | CAS号122-52-1 亚磷酸三乙酯 | CAS号141-52-6 乙醇钠 | CAS号78-39-7 原乙酸三乙酯 | CAS号78-09-1 原碳酸四乙酯 | CAS号1636-15-3 BIS(3,5-DIMETHY... | CAS号60-29-7 乙醚 | CAS号93-89-0 苯甲酸乙酯 | CAS号144175-19-9 N-(diphenylphos... | CAS号4141-48-4 烯丙基联苯氧化膦 | CAS号73207-71-3 1,3-bis(dipheny... | CAS号4559-70-0 二苯基磷氧 | CAS号1733-55-7 二苯基磷酸乙酯 | CAS号6361-05-3 (ETHOXYCARBONYL... | CAS号94-30-4 4-甲氧基苯甲酸乙酯 | CAS号23040-22-4 (DIPHENYLPHOSPH...

合成工艺路线路线简述

    苯基二氯化磷置于aluminum (Iii) Chloride,三乙胺体系中,化学反应生成 二苯基乙氧基膦
    参考文献:在膦酰基部分具有取代基的单酰基氧化膦作为 Norrish I 光引发剂:合成,光引发性质和机理
    标题:在膦酰基部分具有取代基的单酰基氧化膦作为 Norrish I 光引发剂:合成,光引发性质和机理
    摘要:为了研究单酰基氧化膦(mapo)的膦酰基部分的取代基对其稳定性和引发性能的影响,(2,4,6-三甲基苯基)(苯基)(苯甲酰基)氧化膦(tmbpo),(4-甲苯基)(苯基)(2,4,6-三甲基苯甲酰基)氧化膦(4-Mtpo)和(2,4-二甲苯基)(苯基)(2,4,6-三甲基苯甲酰基)氧化膦(2,4-Dmtpo)被设计和准备.对 Tmbpo 的研究表明,将甲基引入 Mapo 的膦酰基部分显着增强了其稳定性和光吸收能力.三羟甲基丙烷三丙烯酸酯 (Tmpta) 的光聚合反应表明,4-Mtpo 和 2,4-Dmtpo 的引发效率高于 Tpo,无论是在 385 Nm 还是 420 Nm 的 Led 上引发.此外,4-Mtpo 和 2 的迁移率,
    DOI:10.1016/j.Jphotochem.2021.113517

    海关参考信息

    专利信息


    专利号:WO-2025082632-A1
    优先权日:2023-10-16
    标 题:Method and composition for oligonucleotide synthesis
    发明人:SAITO MASAHARU
    权利人:BACHEM HOLDING AG
    摘要:The invention pertains to a method for the synthesis of oligonucleotides using pseudo solid-phase protecting groups, wherein said method comprises a step of subjecting a solution comprising a component (C-0)# to one or more aqueous extractions, wherein the organic phase comprises the component (C-0)#. Said component (C-0)# is a nucleoside or an oligonucleotide, which is covalently bonded to a pseudo solid-phase protecting group and comprises a free backbone hydroxyl group. The aqueous phase of each of said one or more aqueous extractions has a pH-value in the range of 4-7.

    专利号:EP-4605403-A1
    优先权日:2022-10-17
    标 题:Method and composition for oligonucleotide synthesis
    发明人:SAITO MASAHARU; TAKEDA KAZUTAKA; OKADA YOHEI; LUTHER ANATOL
    权利人:BACHEM HOLDING AG
    摘要:The invention pertains to methods for the synthesis of oligonucleotides using pseudo solid-phase protecting groups, wherein said method comprises at least one aqueous extraction carried out in the presence of one or more amide solvents SA, wherein each amide solvent SA is an amide solvent comprising one or more alkyl groups, wherein these one or more alkyl groups together comprise in total 6−24 carbon atoms. The invention further pertains to compositions comprising an oligonucleotide which is covalently bonded to a pseudo solid-phase protecting group and a mixed solvent comprising on or more of the aforementioned amide solvents SA.

    专利号:US-2011263870-A1
    优先权日:2010-04-23
    标题 :Novel pyrrole derivatives and their synthesis
    发明人:PRADHAN BRAJA SUNDAR
    权利人:HELVETICA IND P LTD
    摘要:The present invention relates to two novel pyrrole derivatives [3-Phenyl-4-(phenylcarbamoyl)-2-(4-fluorophenyl)-5-(1-methylethyl)-pyrrole-1-yl]methyl(diphenyl)phosphine oxide and Diethyl [3-Phenyl-4-(phenylcarbamoyl)-2-(4-fluorophenyl)-5-(1-methylethyl)-pyrrole-1-yl]methylphosphonate. These pyrrole derivatives can be used as intermediates for the synthesis of the anticholesterol drug atorvastatin.

    专利号:WO-2024083746-A1
    优先权日:2022-10-17
    标 题 :Method and composition for oligonucleotide synthesis
    发明人:SAITO MASAHARU; TAKEDA KAZUTAKA; OKADA YOHEI; LUTHER ANATOL
    权利人:BACHEM HOLDING AG
    摘要:The invention pertains to methods for the synthesis of oligonucleotides using pseudo solid-phase protecting groups, wherein said method comprises at least one aqueous extraction carried out in the presence of one or more amide solvents SA, wherein each amide solvent SA is an amide solvent comprising one or more alkyl groups, wherein these one or more alkyl groups together comprise in total 6−24 carbon atoms. The invention further pertains to compositions comprising an oligonucleotide which is covalently bonded to a pseudo solid-phase protecting group and a mixed solvent comprising on or more of the aforementioned amide solvents SA.

    专利号:US-3992456-A
    优先权日:1969-04-16
    标题:Synthesis of alkadienols
    发明人:ATKINS KENNETH EARL; MANYIK ROBERT MICHAEL; O'CONNOR GEORGE LAWRENCE
    权利人:UNION CARBIDE CORP
    摘要:Alkadienols are prepared by reacting a conjugated diolefin, such as butadiene, with water in the presence of palladium or platinum catalyst and in the presence of solvents. The addition of carbon dioxide to the reaction mixture greatly increases the yield of alkadienols. The products can be hydrogenated to saturated alcohols, useful for making plasticizers.

    专利号:US-12291489-B2
    优先权日:2016-07-01
    标 题 :Synthesis of nanocomposites and their use in enhancing plant nutrition
    发明人:BISWAS PRATIM; RALIYA RAMESH
    权利人:BISWAS PRATIM; RALIYA RAMESH; WASHINGTON UNIVERSITY ST LOUIS
    摘要:The present disclosure is related to the development of improved fertilizer for precision and sustainable agriculture. A method was developed wherein efficient NPK nanocomposite for plant nutrition was synthesized in a single step using aerosol science and technology concepts. Further a formulation was prepared by addition of ZnO, TiO 2 and other nanoparticles to the NPK nanocomposite. Also, an aerosol based foliar application technique was developed for the precise delivery of nanoparticles to the plants.
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    合成参考文献


    摘要:Cacciarini, M.; Larsen, M. H.; Brøndsted Nielsen, M., Science of Synthesis Knowledge Updates, (2015) 2, 302.
    摘要:Demchuk, O. M.; Stankevič, M.; Pietrusiewicz, K. M., Science of Synthesis Knowledge Updates, (2015) 1, 329.
    摘要:Petit, C.; Montchamp, J.-L., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 2, 358.
    参考文献:10.1021/jo0111311
    摘要:Kobayashi T, Eda T, Tamura O, Ishibashi H. Convenient synthesis of 3,3,3-trifluoropropenyl compounds from aromatic aldehydes by means of the TBAF-mediated Horner reaction. J Org Chem. 2002 May 03;67(9):3156–9. doi: 10.1021/jo0111311.
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