2,4,6-tris(4-chlorophenyltelluro)-1,3,5-triazine | 142312-19-4

• 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: 2,4,6-tris(4-chlorophenyltelluro)-1,3,5-triazine
• 英文别名: 2,4,6-tris[(4-chlorophenyl)tellanyl]-1,3,5-triazine
• CAS: 142312-19-4
• 化学式: C₂₁H₁₂Cl₃N₃Te₃
• 分子量: 795.505
• InChiKey: ONOWGESXRVCTPC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  30.0
• 可旋转键数：
  6.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  38.67
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为产物：
  描述：

  三聚氯氰 、 1,2-双(4-氯苯基)二碲化物 在 sodium 作用下， 生成 2,4,6-tris(4-chlorophenyltelluro)-1,3,5-triazine
  参考文献：
  名称：

  Synthesis and Attempted [4+2] Cycloaddition Reaction of 2,4,6-Tris(phenylseleno and aryltelluro)-1,3,5-triazines with Diethyl Acetylenedicarboxylate

  摘要：

  2,4,6-Tris(phenylseleno and aryltelluro)-1,3,5-triazines were synthesized by the reaction of 2,4,6-trichloro-1,3,5-triazine with corresponding arylchalcogenide anions. These 2,4,6-tris(arylchalcogeno)-1,3,5-triazines failed to undergo the Diels-Alder reaction with diethyl acetylenedicarboxylate.

  DOI：

  10.3987/com-91-5926

文献信息

• Synthesis and Attempted [4+2] Cycloaddition Reaction of 2,4,6-Tris(phenylseleno and aryltelluro)-1,3,5-triazines with Diethyl Acetylenedicarboxylate
  作者：Hiroyuki Tani、Tokuo Inamasu、Hitomi Suzuki

  DOI：10.3987/com-91-5926

  日期：——

  2,4,6-Tris(phenylseleno and aryltelluro)-1,3,5-triazines were synthesized by the reaction of 2,4,6-trichloro-1,3,5-triazine with corresponding arylchalcogenide anions. These 2,4,6-tris(arylchalcogeno)-1,3,5-triazines failed to undergo the Diels-Alder reaction with diethyl acetylenedicarboxylate.