CAS: 106-86-5; 3-Vinyl-7-Oxabicyclo[4.1.0]Heptane

该化合物是一种多用途环球环氧环氧化合物,其特点是环氧化合物组和乙烯基功能.这种双功能结构使得它能够作为聚合和交叉结合应用中的活性中间体使用,在治愈的系统中提供强化的热抗力和化学抗药性.该化合物的环氧环已烷主干骨有助于改进僵硬性和稳定性,而该聚乙烯组则为进一步功能化或共聚性提供额外的再活性. 它对于高级涂层,粘合剂和复合材料特别有用,因为需要根据需要定制的机械特性和耐久性. 它的低粘性及其与各种树脂的兼容性进一步增强了其配制设计中的实用性.

结构式图片

相似化合物

1195-92-2 64630-63-3 36099-51-1

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

peracetic acid 4-ethenylcyclohexene 1,1,3,3-tetrachloropropanone acetic acid (2-(7-oxabicyclo[4.1.0]heptan-3-yl)ethyl)triethoxysilane 1,3-bis(2(3,4-epoxycyclohexyl)ethyl)-1,1,3,3-tetramethyldisiloxane 3,4-dihydroxy-1-vinylcyclohexane 4-azido-3-hydroxy-1-vinylcyclohexane

合成工艺路线路线简述

    4-乙烯基-1-环己烯置于过氧乙酸,[mncl2(2-(3-Pyrazolyl)Pyridine)2].h2O体系中,用 乙腈 用作溶剂,化学反应 3.05H,反应生成1,2-环氧-4-乙烯基环己烷
    参考文献:含吡唑基配体的可重复使用的锰化合物,用于烯烃环氧化反应†
    标题:含吡唑基配体的可重复使用的锰化合物,用于烯烃环氧化反应†
    摘要:我们描述了含有二齿配体2-(3-吡唑基)吡啶,Pypz-H和3(5)-(2-羟苯基)吡唑,Hophpz-H的新锰(II)和锰(III)配合物的合成与式[mnx 2(pypz-H)2 ](x =氯-,1,Cf 3 So 3-,2,Oac-,3或no 3-(4)),的mncl 2(pypz-H)( H 2 O)2 ],5或[mncl(ophpz-H)2 ],6.所有的配合物已通过分析,光谱和电化学技术进行了表征.单一x射线结构分析显示,配合物1-5中有六配位的mn(II)离子,而配合物6中有五配位的mn(III)离子.化合物5是含有cl和h 2 O配体以及二齿氮配体的mn(II)的第一共晶体.配合物的催化活性的1-6已经过测试关于苯乙烯的环氧化,并且在的情况下1,5和6,其他烯烃已经在不同的介质中使用过氧乙酸作为氧化剂进行环氧化,其中甘油是一种从未在使用过氧乙酸作为氧化剂的环氧化
    Doi:10.1039/c5Dt02787J

    专利信息


    专利号:WO-2023152730-A1
    优先权日:2022-02-14
    标题 :Amine-borane adducts in the synthesis of polyester and its copolymers using cyclic esters and compositions thereof
    发明人:FENG XIAOSHUANG; LIU JINGJING; GNANOU YVES
    权利人:UNIV KING ABDULLAH SCI & TECH
    摘要:Embodiments of the present disclosure provide for the process of synthesis of polyester and its copolymers through (co)polymerization of cyclic esters and with other oxygenated monomers using amine-borane adduct. Embodiments of the present disclosure further describe the controlled anionic ring-opening polymerization of the cyclic compounds. Embodiments of the present disclosure also describe the polymerization of cyclic compounds using the synergistic effect of amines and thioureas. Embodiments of the present disclosure also describe compositions of polymers formed by the said process.

    专利号:US-5073643-A
    优先权日:1990-08-30
    标 题 :High yield synthesis of hydroxyl-containing cationic photoinitiators
    发明人:CRIVELLO JAMES V
    权利人:POLYSET CORP
    摘要:Synthesis use of a new class of diaryliodonium salt photo and thermal polymerization initiators in which the aryl groups are substituted with alkoxy group bearing hydroxy groups. Good to excellent yields are obtained of diaryliodonium salts in which the aryl groups are substituted with long chain alkoxy groups, which alkoxy groups also possess at least one hydroxyl moiety attached at the 2-position of an alkoxy group. The resultant salts have enhanced solubility when compared with their lower molecular weight counterparts. The hydroxyl groups serve as chain transfer agents; and, in cross linking UV-induced cationic polymerizations, the hydroxyl groups effect marked accelertion on polymerization rates. The salts also have excellent compatability with nonpolar monomers such as epoxidized oil and poly(1,2-butadience oxide) and provide further benefits when they are used along with copper cocatalysts in thermally curable polymer systems. In the latter form of cases, the secondary hydroxyl group serves as a reducing agent for the copper (II) complex.

    专利号:US-2010280189-A1
    优先权日:2005-11-30
    标 题 :Synthesis of cycloaliphatic substituted silane monomers and polysiloxanes for photo-curing
    发明人:DWORAK DAVID P; SOUCEK MARK D
    权利人:UNIV AKRON
    摘要:The present invention generally relates to compositions including linear cycloaliphatic siloxane polymers, and the cyclic cycloaliphatic siloxane oligomers from which they are made. The present invention also generally relates to methods for making cycloaliphatic siloxane polymers, and the cyclic cycloaliphatic siloxane oligomers from which they are made. Some embodiments relate to cationic polymerization of methyl, cyclopentyl, and/or cyclohexyl substituted polysiloxanes. In some embodiments the cationic polymerization is a cationic ring-opening polymerization.

    专利号:US-3979460-A
    优先权日:1974-07-01
    标 题 :Process for the preparation of an organomercaptophenol from sulfur, a 2,6-disubstituted phenol, and an activated olefin or an epoxy compound
    发明人:HAY ALLAN S
    权利人:GEN ELECTRIC
    摘要:A process for the preparation of an organomercaptophenol is described which comprises the reaction of sulfur with a 2,6-disubstituted phenol carried out in the presence of (1) a base, (2) an activated olefin or an epoxy compound, (3) and a solvent with a high dielectric constant. The organomercaptophenols produced by this process are useful as monomers in the synthesis of esters, carbonates, ethers, epoxy compounds, among many other chemicals synthesized from monohydric phenols. In addition, the oganomercaptophenols are also useful as antioxidants.

    专利号:US-4064158-A
    优先权日:1974-07-01
    标题:Process for the preparation of an organomercaptophenol from sulfur, a 2,6-disubstituted phenol, and an activated olefin or an epoxy compound
    发明人:HAY ALLAN S
    权利人:GEN ELECTRIC
    摘要:A process for the preparation of an organomercaptophenol is described which comprises the reaction of sulfur with a 2,6-disubstituted phenol carried out in the presence of (1) a base, (2) an activated olefin or an epoxy compound, (3) and a solvent with a high dielectric constant. The organomercaptophenols produced by this process are useful as monomers in the synthesis of esters, carbonates, ethers, epoxy compounds, among many other chemicals synthesized from monohydric phenols. In addition, the organomercaptophenols are also useful as antioxidants.

    专利号:US-6124418-A
    优先权日:1992-06-11
    标题 :Selective catalysts for the synthesis of epoxysilicone monomers and polymers
    发明人:CRIVELLO JAMES VINCENT; FAN MINGXIN
    权利人:GEN ELECTRIC
    摘要:The invention provides a method for making a curable epoxysilicone composition through the hydrosilation reaction between an ethylenically unsaturated epoxide and an SiH-containing silicone to produce an epoxysilicone product, and catalyzed by a quaternary ammonium, phosphonium or arsonium hexahaloplatinate which does not promote the oxirane ring-opening reaction of either the ethylenically unsaturated epoxide starting material or the epoxysilicone product. The invention also provides for a curable epoxysilicone composition made by the above method.
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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Designing The Synthesis Of Catalytically Active Ti-β By Using Various New Templates In The Presence Of Fluoride Anion
    作者:Manickam Sasidharan,Asim Bhaumik
    摘要:Crystallization Of Large-Pore Ti-î² By Using A Variety Of Diquaternary Ammonium Derivatives Of Dibromoalkane And Amines Such As Triethylamine, 1,4-Diazabicyclo[2,2,2]Octane (Dabco), And Quinuclidine As Structure-Directing Agents (Sda) Is Described. The Size Of Hydrophobic Bridging Alkyl-Chain Length Of The Template [r3N+–(Ch2)X–n+r3](Oh−)2 Directs The Final Crystalline Product: Ti-î², Ti-Zsm-12, Ti-Nonasil Or Ti-Zsm-5, As X Gradually Changes From 6 To 1, In The Fluoride Medium Under Hydrothermal Conditions. A Dense Phase Such As Ti-Nonasil (Clathrasil Type) Is Crystallized As The Size Of Hydrophobic Bridging Alkyl-Chain Length Decreases. The Use Of F− Anions As A Mineralizer And Ti4+ As A Heteroatom In The Synthesis Gel Also Influences The Selectivity Of Final Crystalline Product. The Phase Purity And Incorporation Of Ti4+ Into The Lattice Of î² (Bea) And Zsm-12 Frameworks Are Confirmed Using Xrd, Uv-Visible, Ft-Ir, 29Si Nmr Spectroscopes, Elemental Analysis (Icp), Surface Area Measurements And Catalytic Test Reactions. The Morphology Of Ti-î² Samples Is Dependent On The Nature Of The Structure-Directing Agent As Revealed By The Scanning Electron Microscopic (Sem) Observations. The Catalytic Activity In The Epoxidation Of 4-Vinyl-1-Cyclohexene Is Increased With The Amount Of Tetrahedral Ti4+ Atoms In The Framework. The New Templates Can Be Effectively Used For Preparation Of Catalytically Active Ti-î² With The Minimum Number Of Framework Defect Sites.

    合成参考文献


    摘要:Baudrenghien, L.; Markó, I. E., Science of Synthesis: N-Heterocyclic Carbenes in Catalytic Organic Synthesis, (2016) 1, 309.
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