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2'-benzyloxy-4'-chloroacetophenone | 76292-53-0

中文名称
——
中文别名
——
英文名称
2'-benzyloxy-4'-chloroacetophenone
英文别名
1-(2-(Benzyloxy)-4-chlorophenyl)ethanone;1-(4-chloro-2-phenylmethoxyphenyl)ethanone
2'-benzyloxy-4'-chloroacetophenone化学式
CAS
76292-53-0
化学式
C15H13ClO2
mdl
——
分子量
260.72
InChiKey
NHHMMLDHQLKWKS-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):
    3.7
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2'-benzyloxy-4'-chloroacetophenone 在 selenium(IV) oxide 作用下, 以 戊醇 为溶剂, 反应 50.0h, 以51%的产率得到7-chloro-3',4'-ethylenedioxyflavone
    参考文献:
    名称:
    Chemistry of isoflavone heteroanalogs. 11. Benzodioxane analogs of chalcone, flavone, and isoflavone
    摘要:
    DOI:
    10.1007/bf00519934
  • 作为产物:
    描述:
    4'-氯-2'-羟基苯乙酮氯化苄potassium carbonate 、 potassium iodide 作用下, 以 丙酮 为溶剂, 反应 16.0h, 以59%的产率得到2'-benzyloxy-4'-chloroacetophenone
    参考文献:
    名称:
    Synthesis and Pharmacological Evaluation of Chlorinated N-Alkyl-3- and -5-(2-hydroxyphenyl)pyrazoles as CB 1 Cannabinoid Ligands
    摘要:
    The syntheses of several new 3- and 5-(4-chloro-2-hydroxyphenyl)-5- and -3-(2,4-dichlorophenyl)-1-alkylpyrazoles are reported. These syntheses started from simple chlorophenols, 2,4-dichlorobenzaldehyde or ethyl 2,4-dichlorobenzoate in order to prepare pyrazoles bearing three and four chloro substituents in certain positions. The affinity of these compounds towards the CB1 type cannabinoids receptors was then evaluated in human brain tissues (frontal cortex). The results showed that some of the compounds exhibit affinity towards this kind of receptors in the micromolar range.
    DOI:
    10.1007/s00706-007-0676-4
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文献信息

  • US4265903A
    申请人:——
    公开号:US4265903A
    公开(公告)日:1981-05-05
  • Chemistry of isoflavone heteroanalogs. 11. Benzodioxane analogs of chalcone, flavone, and isoflavone
    作者:V. P. Khilya、A. Aitmambetov、A. V. Turov、A. M. Kornilov、D. Litkei、T. Patonai
    DOI:10.1007/bf00519934
    日期:1986.2
  • Synthesis and Pharmacological Evaluation of Chlorinated N-Alkyl-3- and -5-(2-hydroxyphenyl)pyrazoles as CB 1 Cannabinoid Ligands
    作者:Vera L. M. Silva、Artur M. S. Silva、Diana C. G. A. Pinto、Nadine Jagerovic、Luis F. Callado、José A. S. Cavaleiro、José Elguero
    DOI:10.1007/s00706-007-0676-4
    日期:2007.8
    The syntheses of several new 3- and 5-(4-chloro-2-hydroxyphenyl)-5- and -3-(2,4-dichlorophenyl)-1-alkylpyrazoles are reported. These syntheses started from simple chlorophenols, 2,4-dichlorobenzaldehyde or ethyl 2,4-dichlorobenzoate in order to prepare pyrazoles bearing three and four chloro substituents in certain positions. The affinity of these compounds towards the CB1 type cannabinoids receptors was then evaluated in human brain tissues (frontal cortex). The results showed that some of the compounds exhibit affinity towards this kind of receptors in the micromolar range.
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