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1-(4-methyl-cyclohex-1-enyl)-propan-1-one | 22755-48-2

中文名称
——
中文别名
——
英文名称
1-(4-methyl-cyclohex-1-enyl)-propan-1-one
英文别名
1-(4-Methyl-cyclohex-1-enyl)-propan-1-on;1-Methyl-4-propionyl-cyclohexen-(3);1-Methyl-4-(propylon-(41))-cyclohexen-(3);Aethyl-(4-methyl-cyclohexen-(1)-yl-(1))-keton;1-(4-Methylcyclohexen-1-yl)propan-1-one;1-(4-methylcyclohexen-1-yl)propan-1-one
1-(4-methyl-cyclohex-1-enyl)-propan-1-one化学式
CAS
22755-48-2
化学式
C10H16O
mdl
——
分子量
152.236
InChiKey
ZWVYEKKNKYYGJE-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:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

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文献信息

  • Study of induced hypohalogenation of 1-alkyl(4-methylcyclohex-1-enyl)alkanones, and chemical transformations of the obtained compounds
    作者:O. A. Sadygov
    DOI:10.1134/s1070363209080180
    日期:2009.8
    Induced hydroxyhalogenation of alkyl cyclohexenyl ketones in the systems [MHlg-HX or HHlg]-H2O2 or (NaClO) was performed and the optimal conditions of this reaction were elucidated. It is established that in the system in situ is induced a hypohaloid acid HClO or HBrO is produced that then enters into electrophilic addition at the ring double bond affording hydroxyhalo derivatives of the cycloaliphatic ketones. The alkyl cyclohexenyl ketone chloro(bromo)hydrines and the oxiranes obtained from them are very reactive compounds and can be used as initial compounds for the synthesis of many individual organic compounds
  • Wallach, Justus Liebigs Annalen der Chemie, 1918, vol. 414, p. 227
    作者:Wallach
    DOI:——
    日期:——
  • Wallach; Rentschler, Justus Liebigs Annalen der Chemie, 1908, vol. 360, p. 61
    作者:Wallach、Rentschler
    DOI:——
    日期:——
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