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5,17-dinitro-25,27-bis(benzyloxy)-26,28-bis(chloroformylmethoxy) calix[4]arene | 852402-49-4

中文名称
——
中文别名
——
英文名称
5,17-dinitro-25,27-bis(benzyloxy)-26,28-bis(chloroformylmethoxy) calix[4]arene
英文别名
2-[[27-(2-Chloro-2-oxoethoxy)-11,23-dinitro-26,28-bis(phenylmethoxy)-25-pentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(24),3(28),4,6,9,11,13(27),15,17,19(26),21(25),22-dodecaenyl]oxy]acetyl chloride;2-[[27-(2-chloro-2-oxoethoxy)-11,23-dinitro-26,28-bis(phenylmethoxy)-25-pentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(24),3(28),4,6,9,11,13(27),15,17,19(26),21(25),22-dodecaenyl]oxy]acetyl chloride
5,17-dinitro-25,27-bis(benzyloxy)-26,28-bis(chloroformylmethoxy) calix[4]arene化学式
CAS
852402-49-4
化学式
C46H36Cl2N2O10
mdl
——
分子量
847.705
InChiKey
OVBCOSIJTYCMRE-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):
    11.4
  • 重原子数:
    60
  • 可旋转键数:
    12
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    163
  • 氢给体数:
    0
  • 氢受体数:
    10

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis and characterization of a novel chiral chromogenic calix[4](azoxa)crown-7
    摘要:
    Two new chromogenic compounds, 5 and 6, and a novel chiral chromogenic calix[4](azoxa)crown-7 8 have been synthesized using a calix[4]arene platform. The starting reagents chiral diamine e and calix[4]arene diacid chloride derivative 7 were prepared conveniently according to recent approaches. The H-1 and C-13 NMR, data showed that these compounds exist in a cone conformation. Compounds 5 and 8 have shown broad absorption bands in UV-vis spectra suggesting their utility in different fields, for example, as sensors for ions as well as for chiral molecules. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2004.09.028
  • 作为产物:
    参考文献:
    名称:
    Synthesis and characterization of a novel chiral chromogenic calix[4](azoxa)crown-7
    摘要:
    Two new chromogenic compounds, 5 and 6, and a novel chiral chromogenic calix[4](azoxa)crown-7 8 have been synthesized using a calix[4]arene platform. The starting reagents chiral diamine e and calix[4]arene diacid chloride derivative 7 were prepared conveniently according to recent approaches. The H-1 and C-13 NMR, data showed that these compounds exist in a cone conformation. Compounds 5 and 8 have shown broad absorption bands in UV-vis spectra suggesting their utility in different fields, for example, as sensors for ions as well as for chiral molecules. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2004.09.028
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文献信息

  • Synthesis and characterization of a novel chiral chromogenic calix[4](azoxa)crown-7
    作者:Abdulkadir Sirit、Aysegul Karakucuk、Shahabuddin Memon、Erdal Kocabas、Mustafa Yilmaz
    DOI:10.1016/j.tetasy.2004.09.028
    日期:2004.11
    Two new chromogenic compounds, 5 and 6, and a novel chiral chromogenic calix[4](azoxa)crown-7 8 have been synthesized using a calix[4]arene platform. The starting reagents chiral diamine e and calix[4]arene diacid chloride derivative 7 were prepared conveniently according to recent approaches. The H-1 and C-13 NMR, data showed that these compounds exist in a cone conformation. Compounds 5 and 8 have shown broad absorption bands in UV-vis spectra suggesting their utility in different fields, for example, as sensors for ions as well as for chiral molecules. (C) 2004 Elsevier Ltd. All rights reserved.
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