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2,5-di[5-(3-tert-butyl-2-hydroxybenzaldehyde)]thiophene | 1256124-09-0

中文名称
——
中文别名
——
英文名称
2,5-di[5-(3-tert-butyl-2-hydroxybenzaldehyde)]thiophene
英文别名
3-Tert-butyl-5-[5-(3-tert-butyl-5-formyl-4-hydroxyphenyl)thiophen-2-yl]-2-hydroxybenzaldehyde;3-tert-butyl-5-[5-(3-tert-butyl-5-formyl-4-hydroxyphenyl)thiophen-2-yl]-2-hydroxybenzaldehyde
2,5-di[5-(3-tert-butyl-2-hydroxybenzaldehyde)]thiophene化学式
CAS
1256124-09-0
化学式
C26H28O4S
mdl
——
分子量
436.572
InChiKey
IBAAIQAMBXOPJV-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

物化性质

  • 熔点:
    135 °C
  • 沸点:
    522.1±50.0 °C(predicted)
  • 密度:
    1.202±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.6
  • 重原子数:
    31
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    103
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

点击查看最新优质反应信息

文献信息

  • New Chiral Calixsalen Chromium Complexes: Recyclable Asymmetric Catalysts
    作者:Anaïs Zulauf、Mohamed Mellah、Emmanuelle Schulz
    DOI:10.1002/chem.201001012
    日期:——
    ylenediamine (salen) polymer has been prepared by a condensation reaction between a thiophenedisalicyladehyde derivative and (S,S)‐cyclohexane‐1,2‐diamine. This polymeric compound was demonstrated to possess a cyclic structure with two to five repetitive units. The addition of chromium(II) salts led to the generation of a chiral catalyst that could be recovered as an insoluble powder. The performance
    的手性Ñ,Ñ ' -双(亚水杨基)乙二胺(沙仑)聚合物已经制备由thiophenedisalicyladehyde衍生物和(之间的缩合反应小号,小号)-环己烷-1,2-二胺。证明该聚合化合物具有带有两个至五个重复单元的环状结构。铬(II)盐的添加导致手性催化剂的产生,该手性催化剂可以以不溶性粉末的形式回收。在各种转化中,特别是在异质条件下促进亲核环氧化物开环的能力中,检验了这种新型杯盖型催化剂的性能。与通过使用类似的线性聚合物获得的目标产物相比,以高收率和改进的选择性获得了目标产物。环状结构中催化位点的排列可能更适合于这种苛刻反应的必要的协同双金属途径。该催化剂可以成功地再循环。
  • Synthesis and characterization of original calix–salen type ligands
    作者:Farah Ibrahim、Houssein Nasrallah、Xiang Hong、Mohamed Mellah、Ali Hachem、Ghassan Ibrahim、Nada Jaber、Emmanuelle Schulz
    DOI:10.1016/j.tet.2012.09.077
    日期:2012.12
    Polycondensation reactions between various modified disalicylaldehyde derivatives and two chiral diamines afforded in each case macrocyclic structures, named calix-salen. Mixtures of oligomers (dimers to pentamers) were qualitatively analyzed by Maldi-Tof and H-1 NMR DOSY experiments allowed their easy quantitative investigation. Tuning the reaction conditions and namely the concentration of both monomeric partners led interestingly to the selective preparation of the dimer or the tetramer as main products, in diluted or concentrated media, respectively. (C) 2012 Elsevier Ltd. All rights reserved.
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