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2,4-bis(4-butoxyphenyl)-2,4-dithioxo-1,3,2,4-dithiadiphosphetane | 90058-15-4

中文名称
——
中文别名
——
英文名称
2,4-bis(4-butoxyphenyl)-2,4-dithioxo-1,3,2,4-dithiadiphosphetane
英文别名
2,4-Bis(4-butoxyphenyl)-1,3,2lambda~5~,4lambda~5~-dithiadiphosphetane-2,4-dithione;2,4-bis(4-butoxyphenyl)-2,4-bis(sulfanylidene)-1,3,2λ5,4λ5-dithiadiphosphetane
2,4-bis(4-butoxyphenyl)-2,4-dithioxo-1,3,2,4-dithiadiphosphetane化学式
CAS
90058-15-4
化学式
C20H26O2P2S4
mdl
——
分子量
488.637
InChiKey
KSVWGEUYAZLRIN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    8.6
  • 重原子数:
    28
  • 可旋转键数:
    10
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    133
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

点击查看最新优质反应信息

文献信息

  • 1,2:5,6-Di-<i>O</i>-Cyclohexylidene-<i><scp>d</scp></i>-Mannitol and Its Bis(Trimethylsilyl) Ether in the Dithiophosphorylation Reactions
    作者:Ilyas S. Nizamov、Yevgeniy N. Nikitin、Timur G. Belov、Ilnar D. Nizamov、Alexandra D. Voloshina、Rafael A. Cherkasov
    DOI:10.1002/hc.21307
    日期:2016.3
    The reaction of 2,4-diaryl 1,3,2,4-dithiadiphosphetane-2,4-disulfide with diketonide of d-mannitol has been found to give optically active bisaryldithiophosphonic acids transformed into the corresponding diammonium salts by the treatment of n-hexadecylamine. O,O-Bis(trimethylsilyl) ether of d-mannitol ketonide reacts with 2,4-diaryl 1,3,2,4-dithiadiphosphetane-2,4-disulfide to form chiral S,S-disi
    已发现 2,4-二芳基 1,3,2,4-二硫代二膦烷-2,4-二硫化物与 d-甘露醇的二酮化物的反应得到旋光双芳基二硫代膦酸,通过处理 n-十六胺。d-甘露醇酮的 O,O-双(三甲基甲硅烷基)醚与 2,4-二芳基 1,3,2,4-dithiadiphosphetane-2,4-disulfide 反应形成手性 S,S-二甲硅烷基双芳基二硫代膦酸酯。二芳基二硫代膦酸二铵对金黄色葡萄球菌 ATCC 6538-P 具有抗菌活性。
  • α-<scp>d</scp>-Glucofuranose and α-<scp>d</scp>-allofuranose diacetonides and silyl ether of α-<scp>d</scp>-glucofuranose diacetonide in dithiophosphorylation reactions
    作者:Ilyas S. Nizamov、Yevgeniy N. Nikitin、Ilnar D. Nizamov、Timur G. Belov、Alexandra D. Voloshina、Elvira S. Batyeva、Rafael A. Cherkasov
    DOI:10.1002/hc.21344
    日期:2016.11
    α-d-Glucofuranose and α-d-allofuranose diacetonides react with 2,4-diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides to form optically active dithiophosphonates in 78–81% yields, which are transformed into the corresponding ammonium salts in 90–97% yields by the treatment of n-hexadecylamine. The S-silyldithiophosphonate was prepared in 93% yield by the reaction of 2,4-bis(butoxyphenyl) 1,3,2,4
    α-d-呋喃葡萄糖和 α-d-异呋喃糖二丙酮化物与 2,4-二有机基 1,3,2,4-dithiadiphosphetane-2,4-disulfides 反应生成光学活性二硫代膦酸酯,产率为 78-81%,转化为通过正十六胺的处理,相应的铵盐的产率为 90-97%。S-甲硅烷基二硫代膦酸酯通过 2,4-双(丁氧基苯基)1,3,2,4-二硫代二膦烷-2,4-二硫化物与 α-d-呋喃葡萄糖二丙酮化物的甲硅烷基醚反应制备,产率为 93%。获得的盐之一对金黄色葡萄球菌 ATCC 6538-P 具有抗菌活性。
  • Reactions of 2,4-diaryl 1,3,2,4-dithiadiphosphetane-2,4- disulfides with disilylated resorcinols
    作者:Ilyas S. Nizamov、Yevgeniy N. Nikitin、Ilnar D. Nizamov、Rafael A. Cherkasov
    DOI:10.1080/17415993.2015.1119278
    日期:2016.3.3
    Bis(trimethylsilyl) esters of bisaryldithiophosphonic acids were obtained in 70–81% yields by the reactions of 2,4-diaryl 1,3,2,4-dithiadiphospheta ne-2,4-disulfides with 1,3-bis(trimethylsilyloxy)benzene and 2-methyl 1,3-bis(trimethylsilyloxy)benzene. GRAPHICAL ABSTRACT
    通过 2,4-二芳基 1,3,2,4-二硫二磷酸酯 ne-2,4-二硫化物与 1,3-双(三甲基甲硅烷氧基)的反应,以 70-81% 的产率获得双芳基二硫代膦酸的双(三甲基甲硅烷基)酯苯和 2-甲基 1,3-双(三甲基甲硅烷氧基)苯。图形概要
  • Atropinium dithiophosphates and dithiophosphonates on the basis of α-D-glucofuranose and α-D-galactopyranose diacetonide scaffolds
    作者:Ilyas S Nizamov、Georgiy G Shumatbaev、Ilnar D Nizamov、Varis R Urazbakhtin、Marina P Shulaeva、Oscar K Pozdeev、Elvira S Batyeva
    DOI:10.1007/s12039-023-02224-8
    日期:——
    Optically active dithiophosphoric and dithiophosphonic acids bearing glucofuranose and galactopyranose diacetonide substituents reacted with racemic atropine to give atropinium dithiophosphates or dithiophosphonates as the mixture of diastereomers. Dithiophosphoric and dithiophosphonic acids and their atropinium salts possess antimicrobial activity. Graphical abstract SYNOPSIS: Optically active dithiophosphoric
    带有呋喃葡萄糖和吡喃半乳糖二丙酮化物取代基的光学活性二硫代磷酸和二硫代膦酸与外消旋阿托品反应,得到阿托品二硫代磷酸盐或二硫代磷酸盐,为非对映异构体的混合物。二硫代磷酸和二硫代膦酸及其阿托品盐具有抗菌活性。 图形概要 概要:带有α-D-呋喃葡萄糖和α-D-吡喃半乳糖二丙酮取代基的光学活性二硫代磷酸和二硫代膦酸与外消旋阿托品反应,得到阿托品二硫代磷酸盐或二硫代膦酸盐,为非对映异构体的混合物。二硫代磷酸和二硫代膦酸及其阿托品盐具有抗菌活性。
  • Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol
    作者:I. S. Nizamov、D. A. Terenzhev、I. D. Nizamov、G. G. Shumatbaev、E. S. Batyeva、R. A. Cherkasov
    DOI:10.1134/s1070363216030117
    日期:2016.3
    Carvacrol trimethylsilyl ether when reacting with P4S10 forms S-trimethylsilyl ester of O,O-bis(5-isopropyl-2-methylphenyl)dithiophosphoric acid. The reactions of 2,4-diorganyl-1,3,2,4-dithiadiphosphetane-2,4-disulfides with carvacrol (thymol) trimethylsilyl ether yield the S-trimethylsilyl esters of the corresponding dithiophosphoric acids.
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