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N,2-二甲基氮丙啶-1-甲酰胺 | 73680-89-4

中文名称
N,2-二甲基氮丙啶-1-甲酰胺
中文别名
——
英文名称
N,2-dimethyl-1-aziridinecarboxamide
英文别名
1-(Methylcarbamoyl)-2-methylaziridine;N,2-dimethylaziridine-1-carboxamide
N,2-二甲基氮丙啶-1-甲酰胺化学式
CAS
73680-89-4
化学式
C5H10N2O
mdl
——
分子量
114.147
InChiKey
AXTLSNLDQDWQSJ-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):
    -0.2
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    32.1
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:f44b67a3d39e14151cb92ca525631ffe
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反应信息

  • 作为产物:
    描述:
    异氰酸甲酯2-甲基氮丙啶乙醚 为溶剂, 反应 1.0h, 以80%的产率得到N,2-二甲基氮丙啶-1-甲酰胺
    参考文献:
    名称:
    Synthesis and antineoplastic activity of 1a-formyl and 1a-thioformyl derivatives of mitomycin C and 2-methylaziridine
    摘要:
    A select number of 1-formyl- and 1-thioformyl-2-methylaziridine derivatives and the corresponding 1a-substituted mitomycin C analogues were synthesized and tested for antineoplastic activity by using an in vivo test with murine P388 leukemia. Select compounds were also tested in vivo with murine melanoma B16. Several of the mitomycin C derivatives displayed activity and some of the mitomycin C analogues were comparable in activity to the parent compound.
    DOI:
    10.1021/jm00393a015
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文献信息

  • FISHBEIN, PAUL L.;KOHN, HAROLD, J. MED. CHEM., 30,(1987) N 10, 1767-1773
    作者:FISHBEIN, PAUL L.、KOHN, HAROLD
    DOI:——
    日期:——
  • Synthesis and antineoplastic activity of 1a-formyl and 1a-thioformyl derivatives of mitomycin C and 2-methylaziridine
    作者:Paul L. Fishbein、Harold Kohn
    DOI:10.1021/jm00393a015
    日期:1987.10
    A select number of 1-formyl- and 1-thioformyl-2-methylaziridine derivatives and the corresponding 1a-substituted mitomycin C analogues were synthesized and tested for antineoplastic activity by using an in vivo test with murine P388 leukemia. Select compounds were also tested in vivo with murine melanoma B16. Several of the mitomycin C derivatives displayed activity and some of the mitomycin C analogues were comparable in activity to the parent compound.
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