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1,4,5,8-tetrahydroxanthene | 249284-37-5

中文名称
——
中文别名
——
英文名称
1,4,5,8-tetrahydroxanthene
英文别名
4,5,8,9-tetrahydro-1H-xanthene
1,4,5,8-tetrahydroxanthene化学式
CAS
249284-37-5
化学式
C13H14O
mdl
——
分子量
186.254
InChiKey
XZRXUFHKXZLZAF-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):
    2.5
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    1,4,5,8-tetrahydroxanthene过氧乙酸lithium 、 sodium carbonate 、 氯化铵过碘酸 作用下, 以 四氢呋喃乙醚二氯甲烷 为溶剂, 反应 1.0h, 生成 (Z)-7,10-Dihydro-12H-5-oxa-benzocyclodecene-6,11-dione
    参考文献:
    名称:
    Reduction of Xanteene and the Oxidative Rearrangement of 1,4,5,8-Tetraeydroxanteene to a Spirodiketolactone
    摘要:
    Xanthene (dibenzopyran) was reduced to the corresponding tetrahydro (2) and dihydro (3) ethers. The electrochemical reduction was monitored to determine the optimum yields. 2 was oxidized to the corresponding syn and anti bis epoxides which cleaved and rearranged to 7-oxaspiro[5.8]pentadeca-3,10-dien-1,8,13-trione (6).
    DOI:
    10.1080/00397919908086014
  • 作为产物:
    描述:
    氧杂蒽四丁基氢氧化铵 作用下, 以 为溶剂, 反应 6.0h, 以47%的产率得到1,4,5,8-tetrahydroxanthene
    参考文献:
    名称:
    Reduction of Xanteene and the Oxidative Rearrangement of 1,4,5,8-Tetraeydroxanteene to a Spirodiketolactone
    摘要:
    Xanthene (dibenzopyran) was reduced to the corresponding tetrahydro (2) and dihydro (3) ethers. The electrochemical reduction was monitored to determine the optimum yields. 2 was oxidized to the corresponding syn and anti bis epoxides which cleaved and rearranged to 7-oxaspiro[5.8]pentadeca-3,10-dien-1,8,13-trione (6).
    DOI:
    10.1080/00397919908086014
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文献信息

  • Reduction of Xanteene and the Oxidative Rearrangement of 1,4,5,8-Tetraeydroxanteene to a Spirodiketolactone
    作者:Herbert J. Kaiser、Bradley J. Rowe、David L. Garin
    DOI:10.1080/00397919908086014
    日期:1999.11
    Xanthene (dibenzopyran) was reduced to the corresponding tetrahydro (2) and dihydro (3) ethers. The electrochemical reduction was monitored to determine the optimum yields. 2 was oxidized to the corresponding syn and anti bis epoxides which cleaved and rearranged to 7-oxaspiro[5.8]pentadeca-3,10-dien-1,8,13-trione (6).
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