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2,3-(octa-1,7-diyne-1,8-diyl)-5,6-dimethyl-1,4-benzoquinone | 911820-70-7

中文名称
——
中文别名
——
英文名称
2,3-(octa-1,7-diyne-1,8-diyl)-5,6-dimethyl-1,4-benzoquinone
英文别名
2,3-Dimethyl-5,6,11,12-tetradehydro-7,8,9,10-tetrahydrobenzo[10]annulene-1,4-dione
2,3-(octa-1,7-diyne-1,8-diyl)-5,6-dimethyl-1,4-benzoquinone化学式
CAS
911820-70-7
化学式
C16H14O2
mdl
——
分子量
238.286
InChiKey
VGHRTILPSAXDGR-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:
    118-120 °C (decomp)
  • 沸点:
    360.5±42.0 °C(Predicted)
  • 密度:
    1.18±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2,3-(octa-1,7-diyne-1,8-diyl)-5,6-dimethyl-1,4-benzoquinone1,4-环己二烯 作用下, 以 为溶剂, 反应 5.0h, 以87%的产率得到2,3-dimethyl-5,6,7,8-tetrahydroanthracene-1,4-dione
    参考文献:
    名称:
    Two-Photon Photochemical Generation of Reactive Enediyne
    摘要:
    p-Quinoid cyclopropenone-containing enediyne precursor (1) has been synthesized by monocyclopropanation of one of the triple bonds in p-dimethoxy-substituted 3,4-benzocyclodeca-1,5-diyne followed by oxidative demethylation. Cyclopropenone 1 is stable up to 90 C but readily produces reactive enediyne 2 upon single-photon (Phi(300nm) = 0.46) or two-photon (sigma(800nm) = 0.5 GM) photolysis. The photoproduct 2 undergoes Bergman cyclization at 40 degrees C with the lifetime of 88 h.
    DOI:
    10.1021/jo061285m
  • 作为产物:
    描述:
    2,3-二甲基氢醌 在 bis-triphenylphosphine-palladium(II) chloride 哌啶六甲基磷酰三胺copper(l) iodide正丁基锂 、 ammonium cerium(IV) nitrate 、 potassium carbonate 作用下, 以 四氢呋喃甲醇正己烷氯仿丙酮乙腈 为溶剂, 反应 76.75h, 生成 2,3-(octa-1,7-diyne-1,8-diyl)-5,6-dimethyl-1,4-benzoquinone
    参考文献:
    名称:
    Two-Photon Photochemical Generation of Reactive Enediyne
    摘要:
    p-Quinoid cyclopropenone-containing enediyne precursor (1) has been synthesized by monocyclopropanation of one of the triple bonds in p-dimethoxy-substituted 3,4-benzocyclodeca-1,5-diyne followed by oxidative demethylation. Cyclopropenone 1 is stable up to 90 C but readily produces reactive enediyne 2 upon single-photon (Phi(300nm) = 0.46) or two-photon (sigma(800nm) = 0.5 GM) photolysis. The photoproduct 2 undergoes Bergman cyclization at 40 degrees C with the lifetime of 88 h.
    DOI:
    10.1021/jo061285m
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文献信息

  • Two-Photon Photochemical Generation of Reactive Enediyne
    作者:Andrei Poloukhtine、Vladimir V. Popik
    DOI:10.1021/jo061285m
    日期:2006.9.1
    p-Quinoid cyclopropenone-containing enediyne precursor (1) has been synthesized by monocyclopropanation of one of the triple bonds in p-dimethoxy-substituted 3,4-benzocyclodeca-1,5-diyne followed by oxidative demethylation. Cyclopropenone 1 is stable up to 90 C but readily produces reactive enediyne 2 upon single-photon (Phi(300nm) = 0.46) or two-photon (sigma(800nm) = 0.5 GM) photolysis. The photoproduct 2 undergoes Bergman cyclization at 40 degrees C with the lifetime of 88 h.
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