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Cyclopentylidenecyclohexane | 16189-54-1

中文名称
——
中文别名
——
英文名称
Cyclopentylidenecyclohexane
英文别名
Cyclopentyliden-cyclohexan
Cyclopentylidenecyclohexane化学式
CAS
16189-54-1
化学式
C11H18
mdl
——
分子量
150.264
InChiKey
RBANEFDKYWJMKM-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):
    3.5
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.82
  • 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:
    Cyclopentylidenecyclohexane 生成 6,13,14-Trioxadispiro<4.1.5.2>tetradecan
    参考文献:
    名称:
    GRIESBAUM, KARL;KRIEGER-BECK, PETRA;BECK, JOHANNES, CHEM. BER., 124,(1991) N, C. 391-396
    摘要:
    DOI:
  • 作为产物:
    描述:
    12-Oxa-dispiro[4.0.5.2]tridecan-13-one 生成 Cyclopentylidenecyclohexane
    参考文献:
    名称:
    General synthetic route to cycloalkylidenecycloalkanes. Reactions of .alpha.-anions of cycloalkanecarboxylic acid salts with cycloalkanones
    摘要:
    DOI:
    10.1021/jo00925a010
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文献信息

  • Griesbaum, Karl; Krieger-Beck, Petra; Beck, Johannes, Chemische Berichte, 1991, vol. 124, # 2, p. 391 - 396
    作者:Griesbaum, Karl、Krieger-Beck, Petra、Beck, Johannes
    DOI:——
    日期:——
  • Study of I-Strain Relief in the Intermediate When Forming Spiro Ketones from Unsymmetrical Cycloalkylidenecycloalkanes, Their Dibromides, and Their Pinacols
    作者:Richard D. Sands
    DOI:10.1021/jo00081a030
    日期:1994.1
    Three unsymmetrical intercyclic olefins, their dibromides, and their pinacols were prepared, each so the two carbons involved at the functional group were part of a different sized ring. The pinacols were reacted with 25% sulfuric acid and with boron trifluoride etherate, the dibromides with silver nitrate,and the olefins with mercuric acetate and with trifluoroperacetic acid. The predominant spiro ketone found in each product mixture was used to determine which carbon, and hence which size ring, could better undergo the sp(3) to sp(2) or the sp(2) to sp(3) transition. The findings were consistent with Brown's observations on ring strain.
  • GRIESBAUM, KARL;KRIEGER-BECK, PETRA;BECK, JOHANNES, CHEM. BER., 124,(1991) N, C. 391-396
    作者:GRIESBAUM, KARL、KRIEGER-BECK, PETRA、BECK, JOHANNES
    DOI:——
    日期:——
  • General synthetic route to cycloalkylidenecycloalkanes. Reactions of .alpha.-anions of cycloalkanecarboxylic acid salts with cycloalkanones
    作者:A. Paul Krapcho、E. G. E. Jahngen
    DOI:10.1021/jo00925a010
    日期:1974.6
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