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(4-bromo-butyl)-(2,4,6-trichloro-phenyl)-ether

中文名称
——
中文别名
——
英文名称
(4-bromo-butyl)-(2,4,6-trichloro-phenyl)-ether
英文别名
(4-Brom-butyl)-(2,4,6-trichlor-phenyl)-aether;2.4.6-Trichlor-1-(4-brom-butyloxy)-benzol;4-Brom-1-(2.4.6-trichlor-phenoxy)-butan;4-(2.4.6-Trichlor-phenoxy)-butylbromid;2-(4-Bromobutoxy)-1,3,5-trichlorobenzene
(4-bromo-butyl)-(2,4,6-trichloro-phenyl)-ether化学式
CAS
——
化学式
C10H10BrCl3O
mdl
——
分子量
332.452
InChiKey
XCKQYIFMTALPEY-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):
    5.5
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

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:
    1-(2,4-difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)propan-1-one nitrate 、 (4-bromo-butyl)-(2,4,6-trichloro-phenyl)-ether四丁基氢氧化铵 、 sodium hydroxide 、 硝酸 作用下, 以 甲苯异丙醇 为溶剂, 反应 20.0h, 生成 1-[1-(2,4-difluorophenyl)-1-[4-(2,4,6-trichlorophenoxy)butoxy]prop-1-en-2-yl]-1,2,4-triazole;nitric acid
    参考文献:
    名称:
    Synthesis and biological evaluation of vinyl ether-containing azole derivatives as inhibitors of Trichophyton rubrum
    摘要:
    In an attempt to search for many target compounds with excellent activities, a series of vinyl ether-containing azole derivatives were designed, synthesized, and evaluated as antifungal agents. Results of preliminary antifungal tests against Trichophyton rubrum in vitro indicated that most of the synthesized compounds showed excellent activities. In comparison with fluconazole, itraconazole, voriconazole, omoconazole and amphotericin B, several compounds (such as 7d, 7g and 7h) exhibited more potent inhibitory activities, suggesting that they were promising leads for the development of novel antifungal agents. Crown Copyright (C) 2012 Published by Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.05.070
  • 作为产物:
    参考文献:
    名称:
    ZANKE, D.;EDLICH, W., TAGUNSBER. AKAD. LANDWIRTSCHAFTSWISS. DDR,(1987) N 253, 283-288
    摘要:
    DOI:
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文献信息

  • 564. Antituberculous compounds. Part I. Halogenated ω-aryloxy-alkylamines and analogues
    作者:D. J. Drain、D. A. Peak、F. F. Whitmont
    DOI:10.1039/jr9490002680
    日期:——
  • ZANKE, D.;EDLICH, W., TAGUNSBER. AKAD. LANDWIRTSCHAFTSWISS. DDR,(1987) N 253, 283-288
    作者:ZANKE, D.、EDLICH, W.
    DOI:——
    日期:——
  • Synthesis and biological evaluation of vinyl ether-containing azole derivatives as inhibitors of Trichophyton rubrum
    作者:Lulu Wang、Wenge Yang、Kai Wang、Jing Zhu、Fei Shen、Yonghong Hu
    DOI:10.1016/j.bmcl.2012.05.070
    日期:2012.7
    In an attempt to search for many target compounds with excellent activities, a series of vinyl ether-containing azole derivatives were designed, synthesized, and evaluated as antifungal agents. Results of preliminary antifungal tests against Trichophyton rubrum in vitro indicated that most of the synthesized compounds showed excellent activities. In comparison with fluconazole, itraconazole, voriconazole, omoconazole and amphotericin B, several compounds (such as 7d, 7g and 7h) exhibited more potent inhibitory activities, suggesting that they were promising leads for the development of novel antifungal agents. Crown Copyright (C) 2012 Published by Elsevier Ltd. All rights reserved.
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