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2-methyl-2H-[1,2,3]triazolo[4,5-e][1,2,3,4]tetrazine 1,5,7-trioxide | 1599477-20-9

中文名称
——
中文别名
——
英文名称
2-methyl-2H-[1,2,3]triazolo[4,5-e][1,2,3,4]tetrazine 1,5,7-trioxide
英文别名
2-Methyl-2h-[1,2,3]triazolo[4,5-e]-[1,2,3,4]tetrazine 1,5,7-trioxide;2-methyl-1,5,7-trioxidotriazolo[4,5-e]tetrazine-1,5,7-triium
2-methyl-2H-[1,2,3]triazolo[4,5-e][1,2,3,4]tetrazine 1,5,7-trioxide化学式
CAS
1599477-20-9
化学式
C3H3N7O3
mdl
——
分子量
185.102
InChiKey
LHLVHSQWWJPYHU-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):
    -3.74
  • 重原子数:
    13.0
  • 可旋转键数:
    0.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    124.42
  • 氢给体数:
    0.0
  • 氢受体数:
    7.0

反应信息

  • 作为产物:
    描述:
    4-amino-5-(tert-butyl-NNO-azoxy)-2-methyl-2H-1,2,3-triazole 1-oxide硫酸硝酸乙酸酐 作用下, 以55%的产率得到2-methyl-2H-[1,2,3]triazolo[4,5-e][1,2,3,4]tetrazine 1,5,7-trioxide
    参考文献:
    名称:
    1,2,3-三唑和1,2,3-三唑1-氧化物环化的1,2,3,4-四嗪1,3-二氧化物的合成
    摘要:
    1,2,3,4-四嗪与1,2,3-三唑和1,2,3-三唑环化1,3-二氧化物-1-氧化物已经通过的4-氨基-5-(反应,合成叔-丁基NNO -azoxy)-2-R-2 ħ -1,2,3-三唑(R = Me中,我-Pr,吨-Bu)和它们的1-氧化物(R = H,ME等,我- Pr)和HNO 3 / H 2 SO 4 / Ac 2 O系统。已经研究了它们的热稳定性,光谱学和X射线特性。
    DOI:
    10.1016/j.tet.2014.03.003
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文献信息

  • Efficient methods for the synthesis of 1,2,3,4-tetrazine 1,3-dioxides annulated with five-membered polynitrogen heterocycles
    作者:V. P. Zelenov、M. E. Minyaev
    DOI:10.1007/s11172-021-3094-6
    日期:2021.2
    3-dioxides (TDOs) from appropriate amines based on the annulation with nitronium sulfates in organic solvents and also in HNO3 solutions using weak acid anhydrides. The synthesis of TDOs using P2O5 in an HNO3 solution requires the preliminary thermal decomposition of intermediate nitro(poly)phosphoric acids. The structure of 2-methyl-2H-[1,2,3]triazolo[4,5-e]-[1,2,3,4]tetrazine 1,5,7-trioxide was established
    新的有效方法是为杂环1,2,3,4-四嗪-1,3-二氧化物根据与在有机溶剂中硝硫酸盐的环,并且还以从HNO适当的胺(TDO的)的合成中开发的3种使用弱酸酐溶液。在HNO 3溶液中使用P 2 O 5合成TDO要求对中间体硝基(聚)磷酸进行初步热分解。通过X射线衍射建立了2-甲基-2 H- [1,2,3]三唑并[4,5- e ]-[1,2,3,4]四嗪1,5,7-三氧化物的结构。
  • Synthesis of 1,2,3,4-tetrazine 1,3-dioxides annulated with 1,2,3-triazoles and 1,2,3-triazole 1-oxides
    作者:Alexey A. Voronin、Victor P. Zelenov、Aleksandr M. Churakov、Yurii A. Strelenko、Ivan V. Fedyanin、Vladimir A. Tartakovsky
    DOI:10.1016/j.tet.2014.03.003
    日期:2014.5
    1,2,3,4-Tetrazine 1,3-dioxides annulated with 1,2,3-triazoles and 1,2,3-triazole 1-oxides have been synthesized by the reaction of 4-amino-5-(tert-butyl-NNO-azoxy)-2-R-2H-1,2,3-triazoles (R=Me, i-Pr, t-Bu) and their 1-oxides (R=H, Me, Et, i-Pr) with the HNO3/H2SO4/Ac2O system. Their thermal stability, spectroscopic, and X-ray properties have been studied.
    1,2,3,4-四嗪与1,2,3-三唑和1,2,3-三唑环化1,3-二氧化物-1-氧化物已经通过的4-氨基-5-(反应,合成叔-丁基NNO -azoxy)-2-R-2 ħ -1,2,3-三唑(R = Me中,我-Pr,吨-Bu)和它们的1-氧化物(R = H,ME等,我- Pr)和HNO 3 / H 2 SO 4 / Ac 2 O系统。已经研究了它们的热稳定性,光谱学和X射线特性。
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同类化合物

酸四嗪 甲四嗪-氨基叔丁酯 四嗪-氨基叔丁酯 嘧啶并[4,5-e]-1,2,3,4-四嗪 二甲基-1,2,4,5-四嗪 二氯均四嗪 METHYLTETRAZINE-ACID,甲基四嗪-羧基 6-苯基-1,2,4,5-四嗪-3-胺 6-乙基-1,2,4,5-四嗪-3-胺 6-丁基氨基-3-(3,5-二甲基吡唑-1-基)四嗪 6-(3,5-二甲基吡唑-1-基)-1,2,4,5-四嗪-3-胺 3,6-二苯基-1,2,4,5-四嗪 3,6-二氨基-1,2-二氢-1,2,4,5-四嗪盐酸盐 3,6-二-4-吡啶基-1,2,4,5-四嗪 3,6-二-2-吡啶基-1,2,4,5-四嗪 3,6-二(噻吩-2-基)-1,2,4,5-四嗪 3,6-二(3-吡啶基)-1,2,4,5-四氮杂苯 3,6-二(3,5-二甲基-1H-吡唑-1-基)-1,2,4,5-四嗪 1-[6-(3,5-二甲基吡唑-1-基)-1,2,4,5-四嗪-3-基]-2-(丙-2-亚基)肼 1,2-二氢-1,2,4,5-四嗪-3,6-二酮 1,2,4,5]四嗪-3,6-二羧酸 1,2,4,5-四嗪-3-胺 1,2,4,5-四嗪-3,6-二羧酸二甲酯 1,2,4,5-四嗪 (9CI)-吡咯并[2,1-d]-1,2,3,5-四嗪 (6-肼基-1,2,4,5-四嗪-3-基)肼 3-(3,5-Dimethyl-1-pyrazolyl)-6-(2-trifluoroacetylhydrazino)-1,2,4,5-tetrazine 3-cyclohexyl-6-(3,5-dimethyl-1H-pyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine 3-ethyl-6-(3,5-dimethyl-1H-pyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine 6-pentyl-6-(3,5-dimethyl-1H-pyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine 3-benzyl-6-(3,5-dimethyl-1H-pyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine 3-methyl-6-(3,5-dimethyl-1H-pyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine N'-(6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazin-3-yl)propionohydrazide 3-(2-ethylidenehydrazinyl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazine (1,2,4,5-tetrazine-3,6-diyl)dimethanol 3-amino-6-chloro-1,2,4,5-tetrazine 6-(3,5-dimethyl-1H-pyrazol-1-yl)-N-methyl-1,2,4,5-tetrazin-3-amine N-(tert-butyl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazin-3-amine 6-(3,5-dimethyl-1H-pyrazol-1-yl)-N-(prop-2-en-1-yl)-1,2,4,5-tetrazin-3-amine 3-(2-pyrimidyl)-6-(2-hydroxy)ethyl-1,2,4,5-tetrazine 3-isopropyl-6-phenyl-1,2,4,5-tetrazine 6-butylamino-3-chlorotetrazine 3,6-di(1H-pyrazol-4-yl)-1,2,4,5-tetrazine N-(1H-tetrazol-5-yl)-1,2,4,5-tetrazin-3-amine 3-(3,5-dimethylpyrazolyl)-6-[tris(hydroxylmethyl)aminomethane]-1,2,4,5-tetrazine 2-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-3-ylamino)-2-(hydroxymethyl)propane-1,3-diol 6-amino-1,2,4-triazolo<4,3-b><1,2,4,5>tetrazine N-phenethyl-[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-3-amine 2,5-dioxopyrrolidin-1-yl 2-(4-(6-methyl-1,2,4,5-tetrazin-3-yl)phenyl)acetate furazano-1,2,3,4-tetrazine 1,3-dioxide