CAS: 25990-96-9; 2,5,8,11,14,17,20,23-Octaoxapentacosan-25-Ol

该化合物是合成聚醚化合物,具有长碳链和多醚联系的特点,这种化合物在25碳脊柱内有8个醚(-O-)交叉体,有助于其独特的特性.分子端端中存在氢氧基组(-OH),会增加其在极地溶剂中的溶解性,并可能带来某种程度的水益性.结构表明,它能够展示表面活性特性,使其在各种应用中可能有用,包括乳化剂,洗涤剂或配方中的稳定剂.此外,分子对称和多醚联系的存在可能会影响其热稳定性和机械特性.然而,在不同环境中的具体应用和行为将取决于进一步的经验研究.

结构式图片

相似化合物

1611489-00-9 477775-73-8 25990-94-7

上下游产品

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合成工艺路线路线简述

    2-((2,5,8,11,14,17-Hexaoxanonadecan-19-yl)Oxy)Tetrahydro-2H-Pyran置于盐酸,Sodium Hydride体系中,用 四氢呋喃,甲醇,二氯甲烷 用作溶剂,化学反应生成八甘醇单甲醚
    参考文献:Doubly Activated Supramolecular Reaction: Transesterification Of Acyclic Oligoether Esters With Metal Alkoxides
    标题:Doubly Activated Supramolecular Reaction: Transesterification Of Acyclic Oligoether Esters With Metal Alkoxides
    摘要:Transesterification Reactions Of Acyclic Oligoether Esters E3-E10 With Metal Alkoxides Were Accelerated Upon Noncovalent Complexation Of The Esters With Metal Ions. In The Reaction Of Monovalent Alkaline Metal Alkoxides,Ch3Ona And Ch3Ok,Plots Of The Observed Rate Constants K(Obs) With Respect To The Chain Length Of E3-E10 Showed Selective Acceleration Of The Transesterification. Compared With The Shortest E3,Which Can Hardly Bind Metal Ion,4.3-And 6.6-Fold Accelerations In The Maxima Were Achieved In The Combinations Of E5/ch3Ona And E6/ch3Ok,Respectively. Supramolecular Intermediate Complex Could Be Spectrometrically Visualized By Esi-Ft-Icr-Ms In The Course Of Reaction. Kinetic Experiments,Together With Structural Analyses By Means Of NMR,Mass Spectrometry,And Dft Calculations Of The Intermediate Complexes,Indicate That A Size-Fit Complex Of Host Substitute With Alkali Metal Ion Allows Strong Electron Withdrawing Due To The Close Contact Of The Carbonyl Oxygen To The Metal Ion,Resulting In The Selective Rate Enhancement Of The Reaction,While In The Reaction Of E3-E10 With A Divalent Alkaline Earth Metal Alkoxide,(Ch3-Ch2O)(2)Ba,The K(Obs) Values Increased Stepwise With Elongation Of The Side Arm To Attain An Dramatic Large Acceleration. In Comparison With The K(Obs) Of E3,4610-Fold Acceleration Was Achieved In The Reaction Of E10. The Double Activation Of The Host Substrate And Guest Counter Nucleophile At Once Brings About This Extraordinary Rate Acceleration. The Strong Wrapping Complexation Of Long Oligoether Ester With Barium Ethoxide Allows For The Effective Electron Withdrawal From The Ester Carbonyl Group (Host Activation) As Well As Separation Of The Accompanying Guest Alkoxide Anions (Guest Activation).
    Doi:10.1021/jo102106G

    海关参考信息

    专利信息


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    优先权日:2020-11-20
    标 题:A kind of organic hole transport material and its synthesis method and perovskite battery

    专利号:CN-112500390-B
    优先权日:2020-11-20
    标题 :A kind of organic hole transport material and its synthesis method and perovskite battery
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    主要参考文献


    1: Brown A, Patel S, Ward C, Lorenz A, Ortiz M, DuRoss A, Wieghardt F, Esch A, Otten EG, Heiser LM, Korolchuk VI, Sun C, Sarkar S, Sahay G. PEG-lipid micelles enable cholesterol efflux in Niemann-Pick Type C1 disease-based lysosomal storage disorder. Sci Rep. 2016 Aug 30;6:31750. doi: 10.1038/srep31750.
    2: Saifer MG, Williams LD, Sobczyk MA, Michaels SJ, Sherman MR. Selectivity of binding of PEGs and PEG-like oligomers to anti-PEG antibodies induced by methoxyPEG-proteins. Mol Immunol. 2014 Feb;57(2):236-46. doi: 10.1016/j.molimm.2013.07.014. Epub 2013 Nov 5. doi: 10.1517/17425247.2012.720969. Epub 2012 Aug 30.

    合成参考文献


    摘要:S120 | DUSTCT2024 | Substances from Second NORMAN Collaborative Dust Trial | DOI:10.5281/zenodo.13835254
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