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4-chloro-N-(4-(2-(2,4-dichlorophenoxy)thiazol-5-yl)-2-methylbut-3-yn-2-yl)benzamide | 1354526-26-3

中文名称
——
中文别名
——
英文名称
4-chloro-N-(4-(2-(2,4-dichlorophenoxy)thiazol-5-yl)-2-methylbut-3-yn-2-yl)benzamide
英文别名
4-chloro-N-[4-[2-(2,4-dichlorophenoxy)-1,3-thiazol-5-yl]-2-methylbut-3-yn-2-yl]benzamide
4-chloro-N-(4-(2-(2,4-dichlorophenoxy)thiazol-5-yl)-2-methylbut-3-yn-2-yl)benzamide化学式
CAS
1354526-26-3
化学式
C21H15Cl3N2O2S
mdl
——
分子量
465.787
InChiKey
UUAMHNLJNZGMTO-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):
    6.5
  • 重原子数:
    29
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    79.5
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    2-甲基-3-丁炔-2-胺 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide三乙胺 作用下, 以 四氢呋喃 为溶剂, 反应 3.0h, 生成 4-chloro-N-(4-(2-(2,4-dichlorophenoxy)thiazol-5-yl)-2-methylbut-3-yn-2-yl)benzamide
    参考文献:
    名称:
    Synthesis and Bioactivities of NovelN-(4-(2-Aryloxythiazol-5-yl)but-3-yn-2-yl)benzamides
    摘要:
    AbstractA series of novel N‐(4‐(2‐aryloxythiazol‐5‐yl)but‐3‐yn‐2‐yl)benzamide derivatives were designed and synthesized. Their structures were identified by 1H NMR and elemental analyses. Preliminary bioassays indicated that some title compounds provided >80% control of Sclerotinia sclerotiorum at 50 µg/mL and >70% herbicidal activities against B. campestris at 100 µg/mL. Their structure‐activities relationships were also discussed.
    DOI:
    10.1002/cjoc.201200824
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文献信息

  • Synthesis and Bioactivities of Novel<i>N</i>-(4-(2-Aryloxythiazol-5-yl)but-3-yn-2-yl)benzamides
    作者:Youquan Zhu、Pei Liu、Danyang Wang、Jin Zhang、Jie Cheng、Yuan Ma、Xiaomao Zou、Huazheng Yang
    DOI:10.1002/cjoc.201200824
    日期:2013.2
    AbstractA series of novel N‐(4‐(2‐aryloxythiazol‐5‐yl)but‐3‐yn‐2‐yl)benzamide derivatives were designed and synthesized. Their structures were identified by 1H NMR and elemental analyses. Preliminary bioassays indicated that some title compounds provided >80% control of Sclerotinia sclerotiorum at 50 µg/mL and >70% herbicidal activities against B. campestris at 100 µg/mL. Their structure‐activities relationships were also discussed.
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