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bis(4-formylphenyl) glutarate | 86636-44-4

中文名称
——
中文别名
——
英文名称
bis(4-formylphenyl) glutarate
英文别名
Bis(4-formylphenyl) pentanedioate;bis(4-formylphenyl) pentanedioate
bis(4-formylphenyl) glutarate化学式
CAS
86636-44-4
化学式
C19H16O6
mdl
——
分子量
340.332
InChiKey
GYJJKSQCPAXFBH-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):
    2.3
  • 重原子数:
    25
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    86.7
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    bis(4-formylphenyl) glutarate溶剂黄146 作用下, 以 乙醇 为溶剂, 以95%的产率得到bis(4-((E)-((4-((11-(((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-11-oxoundecyl)oxy)phenyl)imino)methyl)phenyl) glutarate
    参考文献:
    名称:
    Synthesis and Characterization of Cholesterol-Based Tetramers
    摘要:
    Novel symmetrical liquid-crystal tetramers were designed and synthesized. The length of the central spacer and the outer spacers has been varied. The molecular structures of the target compounds were confirmed by Fourier transform infrared and proton nuclear magnetic resonance spectroscopy. The thermal phase behavior of the tetramers was investigated by polarizing optical microscopy and differential scanning calorimetry. All of the liquid-crystal tetramers showed either a chiral nematic mesophase or chiral nematic and smectic mesophases.
    DOI:
    10.1080/15421406.2010.504628
  • 作为产物:
    描述:
    戊二酰基二氯对羟基苯甲醛4-二甲氨基吡啶 作用下, 以 四氢呋喃 为溶剂, 反应 4.0h, 以72%的产率得到bis(4-formylphenyl) glutarate
    参考文献:
    名称:
    Symmetrical dimer liquid crystals derived from benzoxazoles
    摘要:
    A series of dimeric twin liquid crystals derived from symmetric heterocyclic benzoxazoles 1a-1f exhibiting single smectic C phase are reported. All benzoxazoles were prepared by condensation of 2-aminophenols with benzaldehydes and then followed by subsequent intramolecular cyclization. The mesomorphic properties were investigated by DSC and POM, and the structure of the mesophases was confirmed as smectic C phases by powder XRD. The formation of mesophases was attributed to the weak dipole force induced by donor-acceptor interaction (D-A). A monolayer conformation was proposed based on the powder XRD data. A value of aspect ratio d/l=0.80-0.92 was calculated from d-spacings and the molecular lengths. By contrast, the odd-even effects by a value of entropy changes Delta S-SmC -> I/R=2.00-6.50 showing odd-even effect for the transition of SmC -> I phases were also associated in twin system. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.06.001
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文献信息

  • N-BRIDGED POLYNITRONS AND THE USE THEREOF AS CROSS-LINKING AGENTS, IN PARTICULAR IN COATING MATERIALS AND ADHESIVES
    申请人:Dickmeis Marcus
    公开号:US20130018140A1
    公开(公告)日:2013-01-17
    The invention relates to N-bridged polynitrons and their use for cross-linking of unsaturated polymers, as well as a curable composition comprising (a) a N-bridged polynitron, (b) an unsaturated polymer or a mixture of polymers, wherein at least one unsaturated polymer contains unsaturated functions or functional groups which can react with the polynitron, (c) optionally fillers, (d) optionally pigments, (e) optionally additives such as plasticizers, stabilizers, photoinitiators, and (f) optionally, other cross-linking agents such as polyisocyanates, bisdienes, polyoxaziridines, and their use as adhesives, rubber, filling, sprayable thick-layer filler, ink, paint, powder paint, waterborne paint or solvent based paint. Further, the invention relates to cross-linking products obtainable by curing the curable composition according to the present invention.
    该发明涉及N-桥联聚硝基化合物及其在交联不饱和聚合物中的应用,以及包括(a)N-桥联聚硝基化合物、(b)不饱和聚合物或聚合物混合物的可固化组合物,其中至少一种不饱和聚合物含有可以与聚硝基化合物发生反应的不饱和功能或官能团,(c)可选填料,(d)可选颜料,(e)可选添加剂如增塑剂、稳定剂、光引发剂,以及(f)可选其他交联剂如聚异氰酸酯、双二烯、聚噁唑烷等,并将其用作粘合剂、橡胶、填料、喷涂厚层填料、墨水、油漆、粉末涂料、水性涂料或溶剂基涂料。此外,该发明涉及通过固化根据本发明的可固化组合物获得的交联产品。
  • Al-Dujaili, Amar H.; Jenkins, D.; Walton, David R. M., Molecular Crystals and Liquid Crystals (1969-1991), 1988, vol. 164, p. 67 - 76
    作者:Al-Dujaili, Amar H.、Jenkins, D.、Walton, David R. M.
    DOI:——
    日期:——
  • Synthesis and Characterization of Cholesterol-Based Tetramers
    作者:K. C. Majumdar、S. Ponra、S. Chakravorty
    DOI:10.1080/15421406.2010.504628
    日期:2010.10.14
    Novel symmetrical liquid-crystal tetramers were designed and synthesized. The length of the central spacer and the outer spacers has been varied. The molecular structures of the target compounds were confirmed by Fourier transform infrared and proton nuclear magnetic resonance spectroscopy. The thermal phase behavior of the tetramers was investigated by polarizing optical microscopy and differential scanning calorimetry. All of the liquid-crystal tetramers showed either a chiral nematic mesophase or chiral nematic and smectic mesophases.
  • Symmetrical dimer liquid crystals derived from benzoxazoles
    作者:Cheng-Chung Liao、Chung-Shu Wang、Hwo-Shuenn Sheu、Chung K. Lai
    DOI:10.1016/j.tet.2008.06.001
    日期:2008.8
    A series of dimeric twin liquid crystals derived from symmetric heterocyclic benzoxazoles 1a-1f exhibiting single smectic C phase are reported. All benzoxazoles were prepared by condensation of 2-aminophenols with benzaldehydes and then followed by subsequent intramolecular cyclization. The mesomorphic properties were investigated by DSC and POM, and the structure of the mesophases was confirmed as smectic C phases by powder XRD. The formation of mesophases was attributed to the weak dipole force induced by donor-acceptor interaction (D-A). A monolayer conformation was proposed based on the powder XRD data. A value of aspect ratio d/l=0.80-0.92 was calculated from d-spacings and the molecular lengths. By contrast, the odd-even effects by a value of entropy changes Delta S-SmC -> I/R=2.00-6.50 showing odd-even effect for the transition of SmC -> I phases were also associated in twin system. (C) 2008 Elsevier Ltd. All rights reserved.
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