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3,5-dimethyl-1,7-bis(2,4-dinitrophenyl)dipyrazolo<3,4-b;4',3'-e>pyrazine | 180724-46-3

中文名称
——
中文别名
——
英文名称
3,5-dimethyl-1,7-bis(2,4-dinitrophenyl)dipyrazolo<3,4-b;4',3'-e>pyrazine
英文别名
1,7-Bis(2,4-dinitrophenyl)-3,5-dimethyl-1,7-dihydrodipyrazolo[3,4-b:4',3'-e]pyrazine;4,12-bis(2,4-dinitrophenyl)-6,10-dimethyl-2,4,5,8,11,12-hexazatricyclo[7.3.0.03,7]dodeca-1,3(7),5,8,10-pentaene
3,5-dimethyl-1,7-bis(2,4-dinitrophenyl)dipyrazolo<3,4-b;4',3'-e>pyrazine化学式
CAS
180724-46-3
化学式
C20H12N10O8
mdl
——
分子量
520.377
InChiKey
ONZKNFVPCYHGTK-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):
    3.4
  • 重原子数:
    38
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    245
  • 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
  • 下游产品
    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:
    参考文献:
    名称:
    Nitropyrazoles
    摘要:
    Unsubstituted 1H,7H-dipyrazolo[3,4-b-,4',3'-e]pyrazine has been synthesized for the first time starting from 5-amino-3-methyl-1-phenylpyrazole. Its nitration to form C- and N-dinitro-substituted derivatives has been studied. The molecular structure of 3,5-dinitro-1H,7H-dipyrazolo[3,4-b;4',3'-e]pyrazine has been established by X-ray structural investigation; the NH acidity of this compound and the orientation of its alkylation with bromoacetone have also been determined.
    DOI:
    10.1007/bf00702009
  • 作为产物:
    描述:
    3,5-dimethyl-1,7-diphenylbispyrazolo<3,4-b;4',3'-e>pyrazine硫酸硝酸 作用下, 反应 48.0h, 以92%的产率得到3,5-dimethyl-1,7-bis(2,4-dinitrophenyl)dipyrazolo<3,4-b;4',3'-e>pyrazine
    参考文献:
    名称:
    Nitropyrazoles
    摘要:
    Unsubstituted 1H,7H-dipyrazolo[3,4-b-,4',3'-e]pyrazine has been synthesized for the first time starting from 5-amino-3-methyl-1-phenylpyrazole. Its nitration to form C- and N-dinitro-substituted derivatives has been studied. The molecular structure of 3,5-dinitro-1H,7H-dipyrazolo[3,4-b;4',3'-e]pyrazine has been established by X-ray structural investigation; the NH acidity of this compound and the orientation of its alkylation with bromoacetone have also been determined.
    DOI:
    10.1007/bf00702009
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