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5,6,9,10-tetrakis(heptyloxy)-1,3-diphenyl-2H-cyclopenta[l]phenanthren-2-one | 1426954-31-5

中文名称
——
中文别名
——
英文名称
5,6,9,10-tetrakis(heptyloxy)-1,3-diphenyl-2H-cyclopenta[l]phenanthren-2-one
英文别名
5,6,9,10-Tetraheptoxy-1,3-diphenylcyclopenta[l]phenanthren-2-one;5,6,9,10-tetraheptoxy-1,3-diphenylcyclopenta[l]phenanthren-2-one
5,6,9,10-tetrakis(heptyloxy)-1,3-diphenyl-2H-cyclopenta[l]phenanthren-2-one化学式
CAS
1426954-31-5
化学式
C57H74O5
mdl
——
分子量
839.212
InChiKey
WTZXIGAGKULQAU-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

  • 沸点:
    914.3±65.0 °C(predicted)
  • 密度:
    1.09±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    17.5
  • 重原子数:
    62
  • 可旋转键数:
    30
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.49
  • 拓扑面积:
    54
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Fluorogenic Diels–Alder reactions of novel phencyclone derivatives
    摘要:
    With the aim of obtaining fluorogenic Diels-Alder reactions, novel phencyclone derivatives were synthesized. In a short time and under convenient reaction conditions, the formation of Diels-Alder adducts was observed by color-change and up to 33-fold enhancement of fluorescence. The modification of thymidine and deoxycytidine derivatives with a maleimide side chain and their usage in fluorogenic Diels-Alder reaction is also reported. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.01.095
  • 作为产物:
    描述:
    1,2-bis-(3,4-diheptoxyphenyl)ethanedione 在 三氟代氧化钒(V) 、 三氟化硼乙醚 、 potassium hydroxide 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 2.0h, 生成 5,6,9,10-tetrakis(heptyloxy)-1,3-diphenyl-2H-cyclopenta[l]phenanthren-2-one
    参考文献:
    名称:
    Fluorogenic Diels–Alder reactions of novel phencyclone derivatives
    摘要:
    With the aim of obtaining fluorogenic Diels-Alder reactions, novel phencyclone derivatives were synthesized. In a short time and under convenient reaction conditions, the formation of Diels-Alder adducts was observed by color-change and up to 33-fold enhancement of fluorescence. The modification of thymidine and deoxycytidine derivatives with a maleimide side chain and their usage in fluorogenic Diels-Alder reaction is also reported. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.01.095
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文献信息

  • Fluorogenic Diels–Alder reactions of novel phencyclone derivatives
    作者:Engin Aytac Aydin、Hans-Josef Altenbach
    DOI:10.1016/j.tetlet.2013.01.095
    日期:2013.4
    With the aim of obtaining fluorogenic Diels-Alder reactions, novel phencyclone derivatives were synthesized. In a short time and under convenient reaction conditions, the formation of Diels-Alder adducts was observed by color-change and up to 33-fold enhancement of fluorescence. The modification of thymidine and deoxycytidine derivatives with a maleimide side chain and their usage in fluorogenic Diels-Alder reaction is also reported. (C) 2013 Elsevier Ltd. All rights reserved.
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