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ω-(4-Fluorphenoxy)-p-methylacetophenon | 50618-35-4

中文名称
——
中文别名
——
英文名称
ω-(4-Fluorphenoxy)-p-methylacetophenon
英文别名
ω-(4-fluorophenoxy)-p-methylacetophenone;omega-(4-Fluorophenoxy)-p-methylacetophenone;2-(4-fluorophenoxy)-1-(4-methylphenyl)ethanone
ω-(4-Fluorphenoxy)-p-methylacetophenon化学式
CAS
50618-35-4
化学式
C15H13FO2
mdl
MFCD01798408
分子量
244.265
InChiKey
TYLIAPVOZKLSDV-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):
    3.8
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.133
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Compounds including carboxystyrylphenyl group
    摘要:
    苯并呋喃、苯并噻吩和萘并呋喃,它们被羧基苯乙烯基苯基取代,以及它们对应的酯和酰胺是一种光学增白剂,可用于美白和增亮天然和合成纤维、纸张、树脂等。这些化合物可通过苯并呋喃、苯并噻吩或萘并呋喃与芳香醛或最好是其苯胺衍生物相互作用方便地制备。
    公开号:
    US03974144A1
  • 作为产物:
    描述:
    4-氟苯酚2-溴-4'-甲基苯乙酮potassium carbonate 作用下, 以 丁酮 为溶剂, 反应 3.0h, 以76%的产率得到ω-(4-Fluorphenoxy)-p-methylacetophenon
    参考文献:
    名称:
    Synthesis and calcium antagonistic activity of a series of diethyl benzofuryl, benzothienyl and benzogammapyronyl benzylphosphonates
    摘要:
    In this work we present about 15 original heterocyclic diethyl benzylphosphonate analogues of fostedil, in which we have varied the nature of the heterocycle, the substituents or the phosphonic group, or even the position of this latter. Three diethyl 4-(2-benzofuryl) benzyl phosphonates exhibited slightly higher calcium antagonism than the control. Solely substitution with a fluorine atom was able to maintain activity, whereas the other modifications always decreased it.
    DOI:
    10.1016/0223-5234(93)90084-r
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文献信息

  • Compounds including carboxystyrylphenyl group
    申请人:Sterling Drug Inc.
    公开号:US03974144A1
    公开(公告)日:1976-08-10
    Benzofurans, benzothiophenes, and naphthofurans which are substituted by carboxystyrylphenyl groups and their corresponding esters and amides are optical brightening agents useful for whitening and brightening natural and synthetic fibers, papers, resins and the like. The compounds are conveniently prepared by interacting benzofurans, benzothiophenes or naphthofurans, which are substituted by a p-tolyl group, with an aromatic aldehyde or preferably the anil derivative thereof.
    苯并呋喃、苯并噻吩和萘并呋喃,它们被羧基苯乙烯基苯基取代,以及它们对应的酯和酰胺是一种光学增白剂,可用于美白和增亮天然和合成纤维、纸张、树脂等。这些化合物可通过苯并呋喃、苯并噻吩或萘并呋喃与芳香醛或最好是其苯胺衍生物相互作用方便地制备。
  • US3974144A
    申请人:——
    公开号:US3974144A
    公开(公告)日:1976-08-10
  • Synthesis and calcium antagonistic activity of a series of diethyl benzofuryl, benzothienyl and benzogammapyronyl benzylphosphonates
    作者:G Baziard-Mouysset、GW Tchani、JL Stigliani、M Payard、R Bonnafous、J Tisne-Versailles
    DOI:10.1016/0223-5234(93)90084-r
    日期:1993.1
    In this work we present about 15 original heterocyclic diethyl benzylphosphonate analogues of fostedil, in which we have varied the nature of the heterocycle, the substituents or the phosphonic group, or even the position of this latter. Three diethyl 4-(2-benzofuryl) benzyl phosphonates exhibited slightly higher calcium antagonism than the control. Solely substitution with a fluorine atom was able to maintain activity, whereas the other modifications always decreased it.
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