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2-morpholino-4-hydrazino-6-dinitromethyl-1,3,5-triazine | 1445907-97-0

中文名称
——
中文别名
——
英文名称
2-morpholino-4-hydrazino-6-dinitromethyl-1,3,5-triazine
英文别名
——
2-morpholino-4-hydrazino-6-dinitromethyl-1,3,5-triazine化学式
CAS
1445907-97-0
化学式
C8H12N8O5
mdl
——
分子量
300.234
InChiKey
BKLAAFLGVOKELO-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

反应信息

  • 作为反应物:
    描述:
    2-morpholino-4-hydrazino-6-dinitromethyl-1,3,5-triazine 在 potassium hydroxide 作用下, 以 甲醇 为溶剂, 反应 5.0h, 生成
    参考文献:
    名称:
    Synthesis and structure elucidation of novel 5-dinitromethyl-7-alkylamino-1,2,4-triazolo[4,3-a]-1,3,5-triazines
    摘要:
    Synthesis of the novel potassium salts of 5-dinitromethyl-7-alkylamino-1,2,4-triazolo[4,3-a]-1,3,5-triazines 9a-c was performed by heating (in DMSO) 2-alkylamino-4-ethoxymethylidenehydrazino-6-dinitromethyl-1,3,5-triazines 8a-c, obtained by treating of the corresponding 2-alkylamino-4-hydrazino-6-dinitromethyl-1,3,5-triazines 5a-c with orthoformic ester. 2-Alkylamino-4-hydrazino-6-dinitromethyl-1,3,5-triazines were obtained by a sequential substitution of the methoxy groups of the potassium salt of 2,4-dimethoxy-6-dinitromethyl-1,3,5-triazine with an alkylamine (dimethylamine, morpholine, pyrrolidine) and hydrazine. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.05.052
  • 作为产物:
    描述:
    盐酸 作用下, 以 为溶剂, 反应 1.0h, 以89%的产率得到2-morpholino-4-hydrazino-6-dinitromethyl-1,3,5-triazine
    参考文献:
    名称:
    Synthesis and structure elucidation of novel 5-dinitromethyl-7-alkylamino-1,2,4-triazolo[4,3-a]-1,3,5-triazines
    摘要:
    Synthesis of the novel potassium salts of 5-dinitromethyl-7-alkylamino-1,2,4-triazolo[4,3-a]-1,3,5-triazines 9a-c was performed by heating (in DMSO) 2-alkylamino-4-ethoxymethylidenehydrazino-6-dinitromethyl-1,3,5-triazines 8a-c, obtained by treating of the corresponding 2-alkylamino-4-hydrazino-6-dinitromethyl-1,3,5-triazines 5a-c with orthoformic ester. 2-Alkylamino-4-hydrazino-6-dinitromethyl-1,3,5-triazines were obtained by a sequential substitution of the methoxy groups of the potassium salt of 2,4-dimethoxy-6-dinitromethyl-1,3,5-triazine with an alkylamine (dimethylamine, morpholine, pyrrolidine) and hydrazine. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.05.052
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