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1,4-二碘双环[2.2.2]辛烷 | 10364-05-3

中文名称
1,4-二碘双环[2.2.2]辛烷
中文别名
1,4-二碘二环[2.2.2]辛烷
英文名称
1,4-diiodobicyclo<2.2.2>octane
英文别名
1,4-diiodobicyclo[2.2.2]octane;1,4-diiodo-bicyclo<2.2.2>octan;1,4-Dijod-bicyclo<2.2.2>octan;1.4-Dijod-bicyclo<2.2.2>octan;1.4-Dijodobicyclo<2.2.2>octan;1.4-Diiodbicyclo<2.2.2>octan
1,4-二碘双环[2.2.2]辛烷化学式
CAS
10364-05-3
化学式
C8H12I2
mdl
——
分子量
361.992
InChiKey
FWXREWNUAWFVFX-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:
    245-246 °C
  • 沸点:
    300.9±42.0 °C(Predicted)
  • 密度:
    2.20±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.7
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

安全信息

  • 海关编码:
    2903890090

SDS

SDS:8730077d817229edbe7ea25564380518
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Reactions of some bicycloalkyl iodides with bromine
    作者:Kenneth B. Wiberg、William E. Pratt、Michael G. Matturro
    DOI:10.1021/jo00135a007
    日期:1982.7
  • Kopecky, Jan; Smejkal, Jaroslav, Collection of Czechoslovak Chemical Communications, 1980, vol. 45, # 11, p. 2965 - 2970
    作者:Kopecky, Jan、Smejkal, Jaroslav
    DOI:——
    日期:——
  • The di-.pi.-methane rearrangement. 226. Molecular rods: synthesis and properties
    作者:Howard E. Zimmerman、Russell K. King、Michael B. Meinhardt
    DOI:10.1021/jo00046a034
    日期:1992.9
    Our earlier synthetic methodology affording bicyclo[2.2.2]octyl [1]-rod and [2]-rod systems proved inadequate for [41-rods. New synthetic approaches were developed, and [3]- and [41-rod molecules were obtained. Sodium-potassium coupling was employed to afford the longer rod units. A radical anion approach gave lower yields. Hybrid rods with aromatic rings interposed were also synthesized. Rods of 9.2-, 9.7-, 13.4-, 13.9-, and 18.2-angstrom length were included in this study. Consideration of rod chirality suggests each bicyclooctane rod unit to be stereogenic, either P (clockwise) or M (anticlockwise). Thus, in a [1]-rod there are enantiomers and in a [2]-rod there are diastereomers. Molecular mechanics treatment of rod stereoisomerization was carried out. Interconversion of enantiomers of the [l]-rod and diastereomers of the [n]-rods should be very rapid at room temperature. X-ray analysis of the 4,4'-dimethoxy-[2]-rod reveals an achiral conformation. AMI quantum mechanics computations were carried out on [n]-rod radical cations and bridgehead cations.
  • Reaction of 1,4-diiodonorbornane, 1,4-diiodobicyclo[2.2.2]octane, and 1,5-diiodobicyclo[3.2.1]octane with butyllithium. Convenient preparative routes to the [2.2.2]- and [3.2.1]propellanes
    作者:Kenneth B. Wiberg、William E. Pratt、William F. Bailey
    DOI:10.1021/ja00449a045
    日期:1977.3
  • "Mixed staffanes" as intermediate-length staffs for molecular-size tinkertoys. Parent hydrocarbons and terminal diiodides combining bicyclo[1.1.1]pentane with cubane or bicyclo[2.2.2]octane units
    作者:Karin Hassenrueck、Gudipati S. Murthy、Vincent M. Lynch、Josef Michl
    DOI:10.1021/jo00290a036
    日期:1990.2
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