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1-methoxy-1-phenoxypropane

中文名称
——
中文别名
——
英文名称
1-methoxy-1-phenoxypropane
英文别名
1-Methoxypropoxybenzene
1-methoxy-1-phenoxypropane化学式
CAS
——
化学式
C10H14O2
mdl
——
分子量
166.22
InChiKey
JMQMYOILSJWVRE-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):
    2.8
  • 重原子数:
    12
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    甲醇烯丙基苯基醚dicobalt octacarbonyl一氧化碳氢气 作用下, 170.0 ℃ 、6.89 MPa 条件下, 反应 0.5h, 生成 2,2-二甲氧基丙烷1-methoxy-1-phenoxypropane
    参考文献:
    名称:
    A facile synthesis of acetals and aldehydes from allylic ethers catalyzed by cobalt compounds
    摘要:
    Octacarbonyldicobalt has been found to be a very effective catalyst for both converting allylic ethers to their corresponding acetals in the presence of an alcohol and hydrolyzing allylic ethers to aldehydes. High yields(> 95%) were obtained in a very short reaction time under mild carbon monoxide pressure. Iron pentacarbonyl was also found to be an active catalyst but less effective than Co-2(CO)(8).
    DOI:
    10.1016/0022-328x(94)05277-i
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文献信息

  • PROCESS FOR PRODUCING ALISKIREN
    申请人:Chemo Iberica, S.A.
    公开号:EP2576500A2
    公开(公告)日:2013-04-10
  • US4404354A
    申请人:——
    公开号:US4404354A
    公开(公告)日:1983-09-13
  • [EN] PROCESS FOR PRODUCING ALISKIREN<br/>[FR] PROCÉDÉ DE PRODUCTION D'ALISKIREN
    申请人:CHEMO IBERICA SA
    公开号:WO2011151442A2
    公开(公告)日:2011-12-08
    A new route of synthesis of the compound Aliskiren of formula (I), used in the treatment of hypertension, is described.
  • A facile synthesis of acetals and aldehydes from allylic ethers catalyzed by cobalt compounds
    作者:Biau-Hung Chang
    DOI:10.1016/0022-328x(94)05277-i
    日期:1995.4
    Octacarbonyldicobalt has been found to be a very effective catalyst for both converting allylic ethers to their corresponding acetals in the presence of an alcohol and hydrolyzing allylic ethers to aldehydes. High yields(> 95%) were obtained in a very short reaction time under mild carbon monoxide pressure. Iron pentacarbonyl was also found to be an active catalyst but less effective than Co-2(CO)(8).
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