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1,2-bis(4,6-dimethoxy-1,3,5-triazin-2-yl)diazene | 1033125-78-8

中文名称
——
中文别名
——
英文名称
1,2-bis(4,6-dimethoxy-1,3,5-triazin-2-yl)diazene
英文别名
Bis-(4,6-dimethoxy-[1,3,5]triazin-2-yl)-diazene;bis(4,6-dimethoxy-1,3,5-triazin-2-yl)diazene
1,2-bis(4,6-dimethoxy-1,3,5-triazin-2-yl)diazene化学式
CAS
1033125-78-8
化学式
C10H12N8O4
mdl
——
分子量
308.256
InChiKey
JNVXTXUAAWBIEG-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):
    1.7
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    139
  • 氢给体数:
    0
  • 氢受体数:
    12

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

  • 作为反应物:
    描述:
    1,2-bis(4,6-dimethoxy-1,3,5-triazin-2-yl)diazene一水合肼 作用下, 以 乙醇 为溶剂, 反应 4.0h, 以97%的产率得到N,N'-bis(4,6-dimethoxy-1,3,5-triazin-2-yl)hydrazine
    参考文献:
    名称:
    Azo bond hydrogenation with hydrazine, R–NHNH2, and hydrazobenzene
    摘要:
    Hydrogenation of azo bonds with hydrazine, mono-substituted hydrazine, and hydrazobenzene was studied with selected diazene compounds under oxygen-free conditions. The reactions proceed rapidly and in high yield in several solvents, utilizing all N-H protons. While the reduction process is accompanied by the evolution of nitrogen gas in the case of N(2)H(4), the intermediacy of diimide could not be confirmed by standard trapping experiments. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.03.083
  • 作为产物:
    描述:
    N,N'-bis(4,6-dimethoxy-1,3,5-triazin-2-yl)hydrazineN-溴代丁二酰亚胺(NBS) 作用下, 以 乙腈 为溶剂, 反应 2.0h, 以77%的产率得到1,2-bis(4,6-dimethoxy-1,3,5-triazin-2-yl)diazene
    参考文献:
    名称:
    Azo bond hydrogenation with hydrazine, R–NHNH2, and hydrazobenzene
    摘要:
    Hydrogenation of azo bonds with hydrazine, mono-substituted hydrazine, and hydrazobenzene was studied with selected diazene compounds under oxygen-free conditions. The reactions proceed rapidly and in high yield in several solvents, utilizing all N-H protons. While the reduction process is accompanied by the evolution of nitrogen gas in the case of N(2)H(4), the intermediacy of diimide could not be confirmed by standard trapping experiments. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.03.083
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文献信息

  • High-energy 1,3,5-triazinyl diazenes, and process thereof
    申请人:The United States of America as represented by the Secretary of the Navy
    公开号:US07399841B1
    公开(公告)日:2008-07-15
    A compound possesses the chemical structure of: wherein n is greater than zero. The compound is useful in energetic composition, particularly in linear, branched, dendritric, oligomer and cyclic oligomer azo-triazine forms.
    这个化合物的化学结构为:其中n大于零。这个化合物在能量组分中很有用,特别是在线性、分支、树状、寡聚体和环状寡聚体偶氮三嗪形式中。
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