[4-(5-Amino-4,6-diisopropyl-pyridin-2-yloxy)-phenyl]-phenyl-methanone | 133980-61-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: [4-(5-Amino-4,6-diisopropyl-pyridin-2-yloxy)-phenyl]-phenyl-methanone
• CAS: 133980-61-7
• 化学式: C₂₄H₂₆N₂O₂
• 分子量: 374.483
• InChiKey: KHDBYVAQSASCSV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.93
• 重原子数：
  28.0
• 可旋转键数：
  6.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  65.21
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  [4-(5-Amino-4,6-diisopropyl-pyridin-2-yloxy)-phenyl]-phenyl-methanone 在 三乙胺 作用下， 以 吡啶 、 乙醇 、 甲苯 为溶剂， 生成
  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：

  4-羟基-二苯甲酮 在 Ra-Ni 氢气 、 potassium carbonate 作用下， 以 四氢呋喃 、 乙醇 、 二甲基亚砜 为溶剂， 生成 [4-(5-Amino-4,6-diisopropyl-pyridin-2-yloxy)-phenyl]-phenyl-methanone
  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