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2-(5-Methoxy-2-methyl-phenyl)-4,4-dimethyl-3-vinyl-cyclohex-2-enone | 217460-43-0

中文名称
——
中文别名
——
英文名称
2-(5-Methoxy-2-methyl-phenyl)-4,4-dimethyl-3-vinyl-cyclohex-2-enone
英文别名
3-Ethenyl-2-(5-methoxy-2-methylphenyl)-4,4-dimethylcyclohex-2-en-1-one
2-(5-Methoxy-2-methyl-phenyl)-4,4-dimethyl-3-vinyl-cyclohex-2-enone化学式
CAS
217460-43-0
化学式
C18H22O2
mdl
——
分子量
270.371
InChiKey
WTQLHVVJLQKATC-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):
    4.1
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-(5-Methoxy-2-methyl-phenyl)-4,4-dimethyl-3-vinyl-cyclohex-2-enone四氯化钛 作用下, 反应 0.25h, 以83%的产率得到8,8,10a-Trimethyl-7,8,10,10a-tetrahydro-6H,9H-phenanthrene-3,5-dione
    参考文献:
    名称:
    The synthesis of quaternary carbon centers through cyclialkylations
    摘要:
    Treatment of conjugated dienone 1 with at strong Lewis acid at -78 degrees C produced a hydrophenanthrene with a newly created quaternary carbon. During this transformation the arene moiety becomes a dienone system. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(98)01931-5
  • 作为产物:
    描述:
    2-(5-Methoxy-2-methyl-phenyl)-6,6-dimethyl-1-vinyl-cyclohex-2-enol 在 重铬酸吡啶 作用下, 生成 2-(5-Methoxy-2-methyl-phenyl)-4,4-dimethyl-3-vinyl-cyclohex-2-enone
    参考文献:
    名称:
    The synthesis of quaternary carbon centers through cyclialkylations
    摘要:
    Treatment of conjugated dienone 1 with at strong Lewis acid at -78 degrees C produced a hydrophenanthrene with a newly created quaternary carbon. During this transformation the arene moiety becomes a dienone system. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(98)01931-5
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文献信息

  • The synthesis of quaternary carbon centers through cyclialkylations
    作者:George Majetich、Jing Fang
    DOI:10.1016/s0040-4039(98)01931-5
    日期:1998.11
    Treatment of conjugated dienone 1 with at strong Lewis acid at -78 degrees C produced a hydrophenanthrene with a newly created quaternary carbon. During this transformation the arene moiety becomes a dienone system. (C) 1998 Elsevier Science Ltd. All rights reserved.
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