2-(butoxymethyl)oxirane | 7297-11-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 环氧化物
• 英文名称: 2-(butoxymethyl)oxirane
• 英文别名: Amyl-glycidylaether；n-Amylglycidylaether；n-Pentyl-glycidylaether；1,2-epoxy-4-oxanonane；2,3-epoxypropyl pentyl ether；pentyloxymethyl-oxirane；Pentyloxymethyl-oxiran；pentyl glycidyl ether；((Pentyloxy)methyl) oxirane；2-(pentoxymethyl)oxirane
• CAS: 7297-11-2
• 化学式: C₈H₁₆O₂
• 分子量: 144.214
• InChiKey: IQCASZIDTNHBIW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  10
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  21.8
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-(butoxymethyl)oxirane 生成 2-Fluoro-3-pentoxypropan-1-ol
  参考文献：
  名称：

  NOXIRA, XIROYUKI;NAKAMURA, SINITI;KONDO, MARIKO;YAMADA, JOKO

  摘要：

  DOI：
• 作为产物：
  描述：

  戊醇 在 sodium hydroxide 、 乙醚 、 硫酸 作用下， 生成 2-(butoxymethyl)oxirane
  参考文献：
  名称：

  EPOXY ETHERS AND ETHER AMINO ALCOHOLS¹

  摘要：

  DOI：

  10.1021/jo01170a015

文献信息

• ALKALI-DEVELOPABLE PHOTOSENSITIVE RESIN COMPOSITION AND BETA-DIKETONE COMPOUND
  申请人：Yamada Takashi

  公开号：US20100129753A1

  公开（公告）日：2010-05-27

  An alkali developable photosensitive resin composition contains (J) a photopolymerizable unsaturated compound having a structure resulting from the addition reaction of (B) a compound having a β-diketone moiety or a compound having a β-ketoester group to the (meth)acryloyl group of (A) a compound having at least two (meth)acryloyl groups and a hydroxyl group and subsequent esterification of the hydroxyl group of the resulting addition product with (C) a polybasic acid anhydride. The compound having a β-diketone moiety is preferably a novel β-diketone compound represented by general formula (I): wherein R 1 is a C1-C20 alkyl group; R 2 represents R 11 , OR 11 , COR 11 , SR 11 , CONR 12 R 13 , or CN; R 11 , R 12 , and R 13 are each hydrogen, a C1-C20 alkyl group, etc.; a is 0 to 3; and b is 0 to 4.

  一种可由碱显影的光敏树脂组合物，含有（J）一种光聚合不饱和化合物，该化合物的结构是由（B）含β-二酮基团或含β-酮酯基团的化合物与（A）含至少两个(甲基)丙烯酰基团和一个羟基的化合物中的(甲基)丙烯酰基团发生加成反应，并随后将所得加成产物的羟基与（C）多元酸酐进行酯化反应得到的。含β-二酮基团的化合物最好是表示为通用公式（I）的一种新型β-二酮化合物：其中R1是C1-C20烷基团；R2代表R11、OR11、COR11、SR11、CONR12R13或CN；R11、R12和R13分别是氢、C1-C20烷基团等；a是0到3；b是0到4。
• AROMATIC GLYCOL ETHERS AS WRITING MONOMERS IN HOLOGRAPHIC PHOTOPOLYMER FORMULATIONS
  申请人：COVESTRO DEUTSCHLAND AG

  公开号：US20170045816A1

  公开（公告）日：2017-02-16

  The invention relates to a photopolymer formulation comprising specific aromatic glycol ethers as writing monomers, matrix polymers and a photoinitiator. The invention further provides an unexposed holographic medium obtainable using an inventive photopolymer formulation, and an exposed holographic medium obtainable by exposing a hologram into an inventive unexposed holographic medium. The invention likewise provides a visual display comprising an inventive exposed holographic medium, for the use of an inventive exposed holographic medium for production of chip cards, identification documents, 3D images, product protection labels, labels, banknotes or holographic optical elements, and specific aromatic glycol ethers.

  本发明涉及一种光聚合配方，包含特定的芳香族乙二醇醚作为写入单体、基质聚合物和光引发剂。本发明还提供了一种使用创新光聚合配方可获得的未曝光全息介质，以及通过将全息图曝光到创新的未曝光全息介质中获得的曝光全息介质。本发明同样提供了一种包含创新曝光全息介质的视觉显示，用于创新曝光全息介质在生产芯片卡、身份证件、三维图像、产品保护标签、标签、钞票或全息光学元件中的应用，以及特定的芳香族乙二醇醚。
• ORGANIC ELECTRONIC MATERIAL, POLYMERIZATION INITIATOR AND THERMAL POLYMERIZATION INITIATOR, INK COMPOSITION, ORGANIC THIN FILM AND PRODUCTION METHOD FOR SAME, ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, LIGHTING DEVICE, DISPLAY ELEMENT, AND DISPLAY DEVICE
  申请人：Ishitsuka Kenichi

  公开号：US20130037753A1

  公开（公告）日：2013-02-14

  Disclosed is an organic electronic material comprising charge transporting compounds and ionic compounds having electron-accepting properties and high solubility in a solvent. The organic electronic material is characterized by comprising charge transporting compounds and ionic compounds, and in that at least one of the ionic compounds is any one kind of compounds represented by general formulas (1b)-(3b). (In the formulas Y 1 -Y 6 each independently represent a divalent linking group, R 1 -R 6 each independently represent an electron-attracting organic substituent (these structures can further have substituents and hetero-atoms, and R 1 , R 2 and R 3 , or, R 4 -R 6 can respectively combine and become a ring shape or a polymer shape) and L + represents a monovalent cation.)

  本文揭示了一种有机电子材料，包括具有电荷传输化合物和具有接受电子性质且在溶剂中具有高溶解度的离子化合物。该有机电子材料的特点在于包括电荷传输化合物和离子化合物，并且至少其中一个离子化合物是由通用式（1b）-（3b）表示的化合物中的任意一种。（在式中，Y1-Y6分别表示二价连接基团，R1-R6分别表示吸引电子的有机取代基（这些结构可以进一步具有取代基和杂原子，且R1、R2和R3，或者R4-R6可以分别结合形成环状或聚合物形状），L+表示一价阳离子。）
• [EN] NOVEL COMPOUNDS FOR THE TREATMENT OF PARASITIC INFECTIONS<br/>[FR] NOUVEAUX COMPOSÉS POUR LE TRAITEMENT D'INFECTIONS PARASITAIRES
  申请人：GLAXOSMITHKLINE IP DEV LTD

  公开号：WO2019145360A1

  公开（公告）日：2019-08-01

  The present invention relates to novel compounds or pharmaceutically acceptable salts thereof, corresponding compositions, and methods and/or uses in therapy, for example in the treatment of parasitic infections such as malaria, in particular infection by Plasmodium falciparum. (I)

  本发明涉及新化合物或其药用盐，相应的组合物，以及在治疗中的方法和/或用途，例如在治疗寄生虫感染，如疟疾，特别是疟原虫感染方面的应用。
• Catalytic Space Engineering of Porphyrin Metal-Organic Frameworks for Combined CO₂ Capture and Conversion at a Low Concentration
  作者：Jiewei Liu、Yan-Zhong Fan、Xin Li、Yao-Wei Xu、Li Zhang、Cheng-Yong Su

  DOI：10.1002/cssc.201800896

  日期：2018.7.20

  Porous porphyrin metal‐organic frameworks (PMOFs) provide promising platforms for studying CO2 capture and conversion (C3) owing to their versatility in photoelectric, catalytic, and redox activities and porphyrin coordination chemistry. Herein, we report the C3 application of two PMOFs by engineering the coordination space through the introduction of two catalytic metalloporphyrins doped with rhodium

  多孔卟啉金属有机骨架（PMOF）由于具有光电，催化和氧化还原活性以及卟啉配位化学的多功能性，为研究CO 2捕获和转化（C3 ）提供了有前途的平台。在这里，我们通过引入两种掺杂铑或铱的催化金属卟啉，Rh-PMOF- 1和Ir-PMOF- 1，通过工程化配位空间，报告了两种PMOF的C3应用。将CO 2化学固定到环状碳酸酯中，产率高达99％。显着地，催化反应可以在低CO 2下有效地进行浓度和83％和73％高的产率可以在5％CO获得2中的Rh-PMOF-的存在1和Ir-PMOF- 1分别。金属卟啉配体和Zr 6 O 8团簇的协同作用，再加上来自孔隙空间的CO 2浓度效应，可能说明Rh-PMOF- 1在低CO 2浓度下具有出色的催化性能。Rh‐PMOF‐ 1的循环测试表明，运行10次后，催化活性的损失可忽略不计。