2-(3,4-dichlorophenyl)-1,3(2H,4H)-isoquinolinedione | 126070-15-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异喹啉及其衍生物
• 英文名称: 2-(3,4-dichlorophenyl)-1,3(2H,4H)-isoquinolinedione
• 英文别名: 2-(3,4-dichlorophenyl)-4H-isoquinoline-1,3-dione
• CAS: 126070-15-3
• 化学式: C₁₅H₉Cl₂NO₂
• 分子量: 306.148
• InChiKey: LHTLANPJBRGTNN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  20
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  37.4
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-(3,4-dichlorophenyl)-1,3(2H,4H)-isoquinolinedione 生成 2-(3,4-Dichloro-phenyl)-isoquinoline-1,3,4-trione
  参考文献：
  名称：

  Herbicidal activity of 2-substituted 1,3,4-(2H)-isoquinolinetriones

  摘要：

  A series of 2-substituted 1,3,4-isoquinolinetriones (B) 1-15, precursors of the phthalamic acids and of the 1,3-dihydro-1-hydroxy-3-oxo-1-isobenzofurancarboxamides (F), possessing root antigravitropic activities, were prepared and evaluated for herbicidal activity on weeds and crops. Among the compounds examined, several derivatives were very active against weeds, in many cases more active than the commercially available herbicides used as the reference standards. Phytotoxicities on crops, selectivity and persistence of herbicidal effect were observed. (C) 1999 Elsevier Science S.A. All rights reserved.

  DOI：

  10.1016/s0014-827x(99)00037-3
• 作为产物：
  描述：

  邻羧基苯乙酸 、 3,4-二氯苯胺 反应 0.17h， 生成 2-(3,4-dichlorophenyl)-1,3(2H,4H)-isoquinolinedione
  参考文献：
  名称：

  Modena, T.; Azzolina, O.; Genta, I., Il Farmaco, 1989, vol. 44, # 7-8, p. 721 - 730

  摘要：

  DOI：

文献信息

• MODENA, T.;AZZOLINA, O.;GENTA, I.;MAZZA, M., FARMACO, 44,(1989) N-8, C. 721-729
  作者：MODENA, T.、AZZOLINA, O.、GENTA, I.、MAZZA, M.

  DOI：——

  日期：——
• Herbicidal activity of 2-substituted 1,3,4-(2H)-isoquinolinetriones
  作者：Marco Mazza、Tiziana Modena

  DOI：10.1016/s0014-827x(99)00037-3

  日期：1999.6

  A series of 2-substituted 1,3,4-isoquinolinetriones (B) 1-15, precursors of the phthalamic acids and of the 1,3-dihydro-1-hydroxy-3-oxo-1-isobenzofurancarboxamides (F), possessing root antigravitropic activities, were prepared and evaluated for herbicidal activity on weeds and crops. Among the compounds examined, several derivatives were very active against weeds, in many cases more active than the commercially available herbicides used as the reference standards. Phytotoxicities on crops, selectivity and persistence of herbicidal effect were observed. (C) 1999 Elsevier Science S.A. All rights reserved.
• Modena, T.; Azzolina, O.; Genta, I., Il Farmaco, 1989, vol. 44, # 7-8, p. 721 - 730
  作者：Modena, T.、Azzolina, O.、Genta, I.、Mazza, M.

  DOI：——

  日期：——