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methyl 2-isopropoxyacetimidate | 98278-14-9

中文名称
——
中文别名
——
英文名称
methyl 2-isopropoxyacetimidate
英文别名
2-Isopropyloxy-acetimidsaeure-methylester;Isopropyloxy-acetimidsaeure-methylester;Methyl 2-propan-2-yloxyethanimidate
methyl 2-isopropoxyacetimidate化学式
CAS
98278-14-9
化学式
C6H13NO2
mdl
——
分子量
131.175
InChiKey
HULAPGQHZWKPSN-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):
    0.9
  • 重原子数:
    9
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    42.3
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    methyl 2-isopropoxyacetimidate 作用下, 以 乙醇 为溶剂, 反应 48.0h, 生成 4-amino-2-(isopropoxymethyl)pteridine
    参考文献:
    名称:
    Synthesis and potential antiallergic activity of new pteridinones and related compounds
    摘要:
    The synthesis and pharmacological profile of a series of 2-alkoxy and 2-phenoxymethyl-3H-pteridin-4-ones and related compounds are described. These compounds displayed antiallergic activity in the passive cutaneous anaphylaxis test in rats. In contrast to both sodium cromoglycate and nedocromil sodium, many of our compounds were active when administered orally. The most potent in this series, 2-ethoxymethyl-3H-pteridin-4-one 2b (LCB 2183) was investigated in other models of allergy and inflammation. The antiallergic activity was confirmed and interesting antiinflammatory properties were observed. It was therefore selected for further development as a human therapeutic agent.
    DOI:
    10.1016/0223-5234(96)80364-3
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文献信息

  • US5167949A
    申请人:——
    公开号:US5167949A
    公开(公告)日:1992-12-01
  • US5270465A
    申请人:——
    公开号:US5270465A
    公开(公告)日:1993-12-14
  • Synthesis and potential antiallergic activity of new pteridinones and related compounds
    作者:G Ferrand、H Dumas、JC Depin、Y Quentin
    DOI:10.1016/0223-5234(96)80364-3
    日期:1996.1
    The synthesis and pharmacological profile of a series of 2-alkoxy and 2-phenoxymethyl-3H-pteridin-4-ones and related compounds are described. These compounds displayed antiallergic activity in the passive cutaneous anaphylaxis test in rats. In contrast to both sodium cromoglycate and nedocromil sodium, many of our compounds were active when administered orally. The most potent in this series, 2-ethoxymethyl-3H-pteridin-4-one 2b (LCB 2183) was investigated in other models of allergy and inflammation. The antiallergic activity was confirmed and interesting antiinflammatory properties were observed. It was therefore selected for further development as a human therapeutic agent.
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