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2-(3,4-Dichloro-phenyl)-isoquinoline-1,3,4-trione

中文名称
——
中文别名
——
英文名称
2-(3,4-Dichloro-phenyl)-isoquinoline-1,3,4-trione
英文别名
2-(3,4-Dichlorophenyl)isoquinoline-1,3,4-trione
2-(3,4-Dichloro-phenyl)-isoquinoline-1,3,4-trione化学式
CAS
——
化学式
C15H7Cl2NO3
mdl
——
分子量
320.131
InChiKey
SSDFJXRPOMSTQG-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):
    3.6
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    54.4
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    2-(3,4-Dichloro-phenyl)-4-[(Z)-4-dimethylamino-phenylimino]-4H-isoquinoline-1,3-dione 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
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文献信息

  • 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.
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