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1-tert.-butyl-3-[2,4-diisopropyl-6-(4-methoxyphenoxy)-pyrid-3-yl]-thiourea | 133979-40-5

中文名称
——
中文别名
——
英文名称
1-tert.-butyl-3-[2,4-diisopropyl-6-(4-methoxyphenoxy)-pyrid-3-yl]-thiourea
英文别名
1-tert-butyl-3-[2,4-diisopropyl-6-(4-methoxyphenoxy)-pyrid-3-yl]-thiourea;1-Tert-butyl-3-[6-(4-methoxyphenoxy)-2,4-di(propan-2-yl)pyridin-3-yl]thiourea
1-tert.-butyl-3-[2,4-diisopropyl-6-(4-methoxyphenoxy)-pyrid-3-yl]-thiourea化学式
CAS
133979-40-5
化学式
C23H33N3O2S
mdl
——
分子量
415.6
InChiKey
WGLCMUYWXJDYEK-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):
    5.6
  • 重原子数:
    29
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    87.5
  • 氢给体数:
    2
  • 氢受体数:
    4

上下游信息

  • 下游产品
    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-tert.-butyl-3-[2,4-diisopropyl-6-(4-methoxyphenoxy)-pyrid-3-yl]-thiourea2-氯-1-甲基吡啶碘化物三乙胺 作用下, 以 乙腈 为溶剂, 以96%的产率得到1-tert.-butyl-3-[2,4-diisopropyl-6-(4-methoxyphenoxy)-pyrid-3-yl]-carbodiimide
    参考文献:
    名称:
    N-(pyrid-3-yl)thioureas and derivatives as acaricides. I. Synthesis and biological properties
    摘要:
    AbstractIn the course of optimization studies around diafenthiuron, the central aromatic nucleus linked directly to the thiourea unit was replaced by a pyridine moiety. A series of N‐(pyrid‐3‐yl)thioureas, ‐isothioureas and ‐carbodiimides was synthesised and evaluated for acaricidal activity. The synthetic methodology used and the screening results against some spider mites (Tetranychus spp. and Panonychus ssp.) are discussed.
    DOI:
    10.1002/ps.2780420402
  • 作为产物:
    描述:
    2,4-Diisopropyl-6-(4-methoxy-phenoxy)-pyridin-3-ylamine 在 三乙胺 作用下, 以 吡啶甲苯 为溶剂, 生成 1-tert.-butyl-3-[2,4-diisopropyl-6-(4-methoxyphenoxy)-pyrid-3-yl]-thiourea
    参考文献:
    名称:
    N-(pyrid-3-yl)thioureas and derivatives as acaricides. I. Synthesis and biological properties
    摘要:
    AbstractIn the course of optimization studies around diafenthiuron, the central aromatic nucleus linked directly to the thiourea unit was replaced by a pyridine moiety. A series of N‐(pyrid‐3‐yl)thioureas, ‐isothioureas and ‐carbodiimides was synthesised and evaluated for acaricidal activity. The synthetic methodology used and the screening results against some spider mites (Tetranychus spp. and Panonychus ssp.) are discussed.
    DOI:
    10.1002/ps.2780420402
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文献信息

  • US5077304A
    申请人:——
    公开号:US5077304A
    公开(公告)日:1991-12-31
  • <i>N</i>-(pyrid-3-yl)thioureas and derivatives as acaricides. I. Synthesis and biological properties
    作者:Alfons Pascual、Alfred Rindlisbacher
    DOI:10.1002/ps.2780420402
    日期:1994.12
    AbstractIn the course of optimization studies around diafenthiuron, the central aromatic nucleus linked directly to the thiourea unit was replaced by a pyridine moiety. A series of N‐(pyrid‐3‐yl)thioureas, ‐isothioureas and ‐carbodiimides was synthesised and evaluated for acaricidal activity. The synthetic methodology used and the screening results against some spider mites (Tetranychus spp. and Panonychus ssp.) are discussed.
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