CAS: 2238-07-5; 2-(Oxiran-2-Ylmethoxymethyl)Oxirane

该化合物是一种环氧化合物,其特征为两组可进行聚合反应的四氧化合物,这些物质一般是无色的,可粉黄液体或固体,视其配制和温度而定;其粘度相对较低,适合各种应用,特别是在生产环氧树脂方面;DGEBA展示了极好的粘合,化学抗药性和机械性,使它在涂层,粘合剂和复合材料中使用成为理想.该物质的存在有助于其稳定性和再活性,使其能够与硬体交叉,形成耐暖化聚合物.此外,必须谨慎地处理该化合物,因为它可引起皮肤和眼刺激,在使用期间应采取适当的安全措施.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

月桂醇缩水甘油醚 Dodecyl Glycidyl Ether 2461-18-9
烯丙基缩水甘油醚 Allyl Glycidyl Ether 106-92-3

合成工艺路线路线简述

  • 合成目标产物 Diglycidyl Ether 主要起始原料 4-Methoxyphenethyl Alcohol And Epichlorohydrin
  • (文献来源)合成步骤主要原料 4-Methoxyphenethyl Alcohol 和 Epichlorohydrin
📜烯丙基醚置于间氯过氧苯甲酸体系中,用 氯仿 用作溶剂,化学反应生成二缩水甘油醚
参考文献:Nucleophilic Opening Of Bis-Epoxides: A New Access To Symmetrically Functionalised Macrocycles
标题:Nucleophilic Opening Of Bis-Epoxides: A New Access To Symmetrically Functionalised Macrocycles
摘要:A Series Of Polyhydroxylated Symmetrical Macrocycles Has Been Prepared In Satisfactory Yield By 1:1 Condensation Of Several Bis-Epoxides With Various Bis-Nucleophiles. Preliminary Results Are Reported,Which Illustrate The Synthesis Of Crown Ethers And Oxa-Azacrown And Oxa-Thiacrown Compounds. (C) 2000 Elsevier Science Ltd. All Rights Reserved.
Doi:10.1016/s0040-4039(99)02219-4

海关参考信息

专利信息


专利号:US-8748660-B2
优先权日:2012-07-09
标题:Process for the synthesis of antiepileptic drug lacosamide
发明人:MURUGAN MUTHUKRISHNAN; MUJAHID MOHAMMAD; MAJUMDAR PRASHANT PRAMOD
权利人:MURUGAN MUTHUKRISHNAN; MUJAHID MOHAMMAD; MAJUMDAR PRASHANT PRAMOD; COUNCIL SCIENT IND RES
摘要:The present invention relates to the improved and efficient process for the synthesis of antiepileptic drug Lacosamide in high enantiopurity (>98% ee) and better yield. More particularly, the present invention relates to improved and efficient, cost effective process for synthesis of desired (R) isomer of Lacosamide starting from commercially available (S)-benzyl glycidyl ether.

专利号:WO-9900440-A1
优先权日:1997-06-26
标 题:Synthesis of a dendritic polyalcohol
发明人:IHRE HENRIK; HULT ANDERS
权利人:PERSTORP AB; IHRE HENRIK; HULT ANDERS
摘要:A process for a double stage convergent synthesis of a polymeric polyalcohol substantially and preferably built up from polyester units and composed of a monomeric or polymeric core to which at least one hyperbranched dendritic branch (dendron) consisting of a number of branching generations is added. The branching generations comprise a polymeric or monomeric branching chain extender having three reactive functions of which two are hydroxyl groups and one is a carboxyl group. The two hydroxyl groups of the branching chain extender is in a first step ketal protected by reacting said two hydroxyl groups with a ketal. A second step includes protection of the carboxyl group of said branching chain extender. The ketal protected branching chain extender and the carboxyl protected chain extender are then employed for repeated addition in a number of step yielding a predetermined number of branching generations. The thus synthesized dendron is finally added to a core having reactive hydroxyl or epoxide groups and the ketal protected hydroxyl groups are optionally deprotected.

专利号:US-9475757-B2
优先权日:2013-05-03
标 题 :Synthesis of anti-Parkinson agent
发明人:MUTHUKRISHNAN MURUGAN; MUJAHID MOHAMMAD
权利人:COUNCIL SCIENT IND RES
摘要:The present invention relates to an improved process for synthesis of anti-Parkinson compound of formula (I) from commercially available (R)-benzyl glycidyl ether, wherein the compound obtained has enantiopurity greater than >98%. Formula (I) wherein R 1 and R 2 are each independently selected from hydrogen or halogen.

专利号:US-6217901-B1
优先权日:1999-05-25
标题:Liposome-assisted synthesis of polymeric nanoparticles
发明人:PERROTT MICHAEL G; BARRY STEPHEN E
权利人:ALNIS LLC
摘要:Synthetic polymer complements (SPCs) are provided, as well as methods for their synthesis and use. The SPCs range in size from about 20 to about 1000 nm. The SPCs have surfaces that are complementary to surface sites of target molecules, resulting in the ability of the SPCs to selectively bind to molecular targets. The molecular recognition capability of these particles enables their use in diagnostic, therapeutic, and separation applications. The SPC is formed by contacting a target template molecule with a set of building blocks solubilized in the interior of a liposome, which building blocks are then polymerized into a network to form the synthetic polymer complement in the interior of the liposome. The target templates are removed to produce complementary sites in a SPC that map the surface of the target, resulting in a water-soluble SPC nanoparticle of similar dimensions as the interior of the liposome that originally supported it and capable of molecular recognition.

专利号:US-9862687-B2
优先权日:2013-11-15
标题:Morphic forms of hexadecyloxypropyl-phosphonate esters and methods of synthesis thereof
发明人:WARE JR ROY WENDELL; DOWNEY AARON LEIGH
权利人:CHIMERIX INC; CHIMERIX INC
摘要:The disclosure describes methods of synthesis of phosphonate ester compounds. The methods according to the disclosure allow for large-scale preparation of phosphonate ester compounds having high purity and stability. Also disclosed are morphic forms of phosphonate ester compounds.

专利号:WO-9013609-A1
优先权日:1989-05-01
标题 :Novel fluorescent pigment compositions and a process for their preparation and use of same
发明人:MALLAVARAPU LEO X
权利人:MALLAVARAPU LEO X
摘要:A process is disclosed for producing novel fluorescent pigment compositions with no formaldehyde or para-formaldehyde during their synthesis. The synthesis of these compositions is, for example, achieved by using an in situ reaction of epoxy resins of preferably up to a molecular weight of 20,000 with a sulfonamide compound, e.g., toluene sulfonamide, in the presence of a Lewis acid catalyst, followed by, preferably, the further reaction with an isocyanate, e.g., aliphatic isocyanate and/or para-toluene sulfonyl isocyanate. During this reaction, a fluorescent dye is incorporated into the molten mass.

供应商参考报价(招募中)

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

合成参考文献


参考文献:10.1007/s11095-005-8924-y
摘要:Rodriguez-Tenreiro C, Alvarez-Lorenzo C, Rodriguez-Perez A, Concheiro A, Torres-Labandeira JJ. New cyclodextrin hydrogels cross-linked with diglycidylethers with a high drug loading and controlled release ability. Pharm Res. 2006 Jan;23(1):121–30. doi: 10.1007/s11095-005-8924-y.
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