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2,3,6,7-tetrakis(heptyloxy)phenanthrene-9,10-dione | 1426954-30-4

中文名称
——
中文别名
——
英文名称
2,3,6,7-tetrakis(heptyloxy)phenanthrene-9,10-dione
英文别名
2,3,6,7-Tetraheptoxyphenanthrene-9,10-dione;2,3,6,7-tetraheptoxyphenanthrene-9,10-dione
2,3,6,7-tetrakis(heptyloxy)phenanthrene-9,10-dione化学式
CAS
1426954-30-4
化学式
C42H64O6
mdl
——
分子量
664.967
InChiKey
OCEAPSDWPMTORS-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):
    14
  • 重原子数:
    48
  • 可旋转键数:
    28
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    71.1
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    2,3,6,7-tetrakis(heptyloxy)phenanthrene-9,10-dione 在 potassium hydroxide 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 1.5h, 生成
    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 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以75%的产率得到2,3,6,7-tetrakis(heptyloxy)phenanthrene-9,10-dione
    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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