摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-[2-(3-methoxy-phenyl)-ethyl]-cyclohex-2-enone | 82586-29-6

中文名称
——
中文别名
——
英文名称
3-[2-(3-methoxy-phenyl)-ethyl]-cyclohex-2-enone
英文别名
3-[2-(3-Methoxyphenyl)ethyl]-2-cyclohexen-1-one;3-[2-(3-methoxyphenyl)ethyl]cyclohex-2-en-1-one
3-[2-(3-methoxy-phenyl)-ethyl]-cyclohex-2-enone化学式
CAS
82586-29-6
化学式
C15H18O2
mdl
——
分子量
230.307
InChiKey
LUFNIDZRTCLNIK-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):
    2.6
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 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:
    3-[2-(3-methoxy-phenyl)-ethyl]-cyclohex-2-enonesodium hydroxide双氧水 作用下, 以 甲醇 为溶剂, 以80%的产率得到6-[2-(3-Methoxy-phenyl)-ethyl]-7-oxa-bicyclo[4.1.0]heptan-2-one
    参考文献:
    名称:
    An approach to the phenanthrene nucleus via thionium ions and epoxyketone cyclizations
    摘要:
    DOI:
    10.1016/s0040-4039(00)87018-5
  • 作为产物:
    描述:
    间甲氧基苯乙基溴2,6-二甲基吡啶 、 lithium perchlorate 、 magnesium 作用下, 以 四氢呋喃 为溶剂, 反应 27.5h, 生成 3-[2-(3-methoxy-phenyl)-ethyl]-cyclohex-2-enone
    参考文献:
    名称:
    Two-Step Electrochemical Annulation for the Assembly of Polycyclic Systems
    摘要:
    [GRAPHIC]A two-step electrochemical annulation has been developed for the preparation of fused furans. The process involves an initial conjugate addition of a furyethyl cuprate and trapping of the enolate as the corresponding silyl enolether. The second step of the annulation involves the anodic coupling of the furan and the silyl enol ether to form a six-membered ring.
    DOI:
    10.1021/ol026771k
点击查看最新优质反应信息

文献信息

  • A Convergent Synthesis of Functionalized B-seco Taxane Skeletons
    作者:C Montalbetti
    DOI:10.1016/00404-0399(50)1172e-
    日期:1995.8.14
  • Two-Step Electrochemical Annulation for the Assembly of Polycyclic Systems
    作者:Christopher R. Whitehead、E. Hampton Sessions、Ion Ghiviriga、Dennis L. Wright
    DOI:10.1021/ol026771k
    日期:2002.10.1
    [GRAPHIC]A two-step electrochemical annulation has been developed for the preparation of fused furans. The process involves an initial conjugate addition of a furyethyl cuprate and trapping of the enolate as the corresponding silyl enolether. The second step of the annulation involves the anodic coupling of the furan and the silyl enol ether to form a six-membered ring.
  • An approach to the phenanthrene nucleus via thionium ions and epoxyketone cyclizations
    作者:Barry M. Trost、Eigoro Murayama
    DOI:10.1016/s0040-4039(00)87018-5
    日期:1982.1
查看更多