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1,8-Dimethylene-1,2,3,4,5,6,7,8-octahydro-anthracene | 864851-82-1

中文名称
——
中文别名
——
英文名称
1,8-Dimethylene-1,2,3,4,5,6,7,8-octahydro-anthracene
英文别名
4,5-Dimethylidene-1,2,3,6,7,8-hexahydroanthracene;4,5-dimethylidene-1,2,3,6,7,8-hexahydroanthracene
1,8-Dimethylene-1,2,3,4,5,6,7,8-octahydro-anthracene化学式
CAS
864851-82-1
化学式
C16H18
mdl
——
分子量
210.319
InChiKey
MPBGLCCMUOLFST-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):
    4.4
  • 重原子数:
    16
  • 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:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    1,8-Dimethylene-1,2,3,4,5,6,7,8-octahydro-anthracene二碘甲烷diethylzinc 作用下, 以24%的产率得到2',3',4',5',6',7'-hexahydrodispiro[cyclopropane-1,1'-anthracene-8',1''-cyclopropane]
    参考文献:
    名称:
    A hydrogen atom sandwiched by cyclopropanes
    摘要:
    2',3',4',5',6',7'-Hexahydrodispiro[cyclopropane-1,1 '-anthracene-8',1"-eyelopropane] (1) was prepared by double olefination (Wittig) and double methylenation (Furukawa) of 1,8-dioxo- 1,2,3,4,5,6,7,8 - octahydroanthracene (4) that was in turn prepared in two steps from 1,3-dibromobenzene. The X-ray structure of 1 shows that the C-9-H of its anthracene core is located 2.6 angstrom from the centroids of each of the flanking cyclopropane rings. The H-1 NMR spectrum of 1 shows that the C-9-H resonance (delta 5.95) falls 0.84 ppm upfield from the C-10-H resonance (delta 6.79). (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2005.07.097
  • 作为产物:
    描述:
    Dimethyl-m-benzoldibutanat 在 氢氧化钾 作用下, 以 为溶剂, 生成 1,8-Dimethylene-1,2,3,4,5,6,7,8-octahydro-anthracene
    参考文献:
    名称:
    A hydrogen atom sandwiched by cyclopropanes
    摘要:
    2',3',4',5',6',7'-Hexahydrodispiro[cyclopropane-1,1 '-anthracene-8',1"-eyelopropane] (1) was prepared by double olefination (Wittig) and double methylenation (Furukawa) of 1,8-dioxo- 1,2,3,4,5,6,7,8 - octahydroanthracene (4) that was in turn prepared in two steps from 1,3-dibromobenzene. The X-ray structure of 1 shows that the C-9-H of its anthracene core is located 2.6 angstrom from the centroids of each of the flanking cyclopropane rings. The H-1 NMR spectrum of 1 shows that the C-9-H resonance (delta 5.95) falls 0.84 ppm upfield from the C-10-H resonance (delta 6.79). (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2005.07.097
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文献信息

  • A hydrogen atom sandwiched by cyclopropanes
    作者:Robert S. Walters、Douglas M. Ho、Robert A. Pascal
    DOI:10.1016/j.tetlet.2005.07.097
    日期:2005.9
    2',3',4',5',6',7'-Hexahydrodispiro[cyclopropane-1,1 '-anthracene-8',1"-eyelopropane] (1) was prepared by double olefination (Wittig) and double methylenation (Furukawa) of 1,8-dioxo- 1,2,3,4,5,6,7,8 - octahydroanthracene (4) that was in turn prepared in two steps from 1,3-dibromobenzene. The X-ray structure of 1 shows that the C-9-H of its anthracene core is located 2.6 angstrom from the centroids of each of the flanking cyclopropane rings. The H-1 NMR spectrum of 1 shows that the C-9-H resonance (delta 5.95) falls 0.84 ppm upfield from the C-10-H resonance (delta 6.79). (c) 2005 Elsevier Ltd. All rights reserved.
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