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4-(4-chlorobenzyl)-5,8-dichloro-2H-phthalazin-1-one | 1132953-80-0

中文名称
——
中文别名
——
英文名称
4-(4-chlorobenzyl)-5,8-dichloro-2H-phthalazin-1-one
英文别名
——
4-(4-chlorobenzyl)-5,8-dichloro-2H-phthalazin-1-one化学式
CAS
1132953-80-0
化学式
C15H9Cl3N2O
mdl
——
分子量
339.608
InChiKey
ZYCSZTJJGKGTAK-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):
    4.47
  • 重原子数:
    21.0
  • 可旋转键数:
    2.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    45.75
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    2-肼基乙醇4-(4-chlorobenzyl)-5,8-dichloro-2H-phthalazin-1-one 以55%的产率得到6-chloro-5-(4-chlorobenzyl)-1-(2-hydroxyethyl)-3H-1,3-dihydropyrazolo[3,4,5-de]phthalazine
    参考文献:
    名称:
    Pyrazolo[3,4,5-de]phthalazine. Syntheses of a practically unknown heterocyclic system
    摘要:
    Simple procedures for the synthesis of 1,3-dihydropyrazolo[3,4,5-de]phthalazines (2), a practically novel type of heterocyclic compounds, have been developed. Compounds equally substituted at positions N-1 and N-3 can be directly obtained from 4,7-dihalogenated benzalphthalides (1). Those with different R-2 and R-3 substituents are prepared through intermediate phthalazin-1-ones (3), whose synthesis is also considered. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.12.072
  • 作为产物:
    描述:
    4,7-dichloro-3-(4-chlorobenzylidene)-3H-isobenzofuran-1-onesilica gel一水合肼 作用下, 反应 0.01h, 以54%的产率得到2-amino-4,7-dichloro-3-(4-chlorobenzyl)-3-hydroxyisoindolin-1-one
    参考文献:
    名称:
    Pyrazolo[3,4,5-de]phthalazine. Syntheses of a practically unknown heterocyclic system
    摘要:
    Simple procedures for the synthesis of 1,3-dihydropyrazolo[3,4,5-de]phthalazines (2), a practically novel type of heterocyclic compounds, have been developed. Compounds equally substituted at positions N-1 and N-3 can be directly obtained from 4,7-dihalogenated benzalphthalides (1). Those with different R-2 and R-3 substituents are prepared through intermediate phthalazin-1-ones (3), whose synthesis is also considered. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.12.072
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