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m-allyloxy-benzimidic acid ethyl ester | 55308-49-1

中文名称
——
中文别名
——
英文名称
m-allyloxy-benzimidic acid ethyl ester
英文别名
Ethyl 3-prop-2-enoxybenzenecarboximidate
m-allyloxy-benzimidic acid ethyl ester化学式
CAS
55308-49-1
化学式
C12H15NO2
mdl
——
分子量
205.257
InChiKey
IEKHYRHQKHZFSD-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):
    2.8
  • 重原子数:
    15
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 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:
    参考文献:
    名称:
    A new class of nonhormonal pregnancy-terminating agents. Synthesis and contragestational activity of 3,5-diaryl-s-triazoles
    摘要:
    A series of 3,5-diaryl-s-triazoles were synthesized and evaluated as postimplantation contragestational agents. The introduction of various substituents (e.g., an o-alkyl chain on one phenyl and a m-alkoxy group on the other) was found to increase the potency. Several compounds with very high pregnancy-terminating activity in both hamsters and rats were obtained. One of these, 3-(2-ethylphenyl)-5-(3-methoxyphenyl)-s-triazole, DL 111 (36), was selected for detailed evaluation in various animal species. A synthetic scheme for the preparation of these compounds and preliminary structure-activity relationships are presented.
    DOI:
    10.1021/jm00362a018
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文献信息

  • OMODEI-SALE, A.;CONSONNI, P.;GALLIANI, G., J. MED. CHEM., 1983, 26, N 8, 1187-1192
    作者:OMODEI-SALE, A.、CONSONNI, P.、GALLIANI, G.
    DOI:——
    日期:——
  • US4379155A
    申请人:——
    公开号:US4379155A
    公开(公告)日:1983-04-05
  • US4370336A
    申请人:——
    公开号:US4370336A
    公开(公告)日:1983-01-25
  • A new class of nonhormonal pregnancy-terminating agents. Synthesis and contragestational activity of 3,5-diaryl-s-triazoles
    作者:Amedeo Omodei-Sale、Pietro Consonni、Giulio Galliani
    DOI:10.1021/jm00362a018
    日期:1983.8
    A series of 3,5-diaryl-s-triazoles were synthesized and evaluated as postimplantation contragestational agents. The introduction of various substituents (e.g., an o-alkyl chain on one phenyl and a m-alkoxy group on the other) was found to increase the potency. Several compounds with very high pregnancy-terminating activity in both hamsters and rats were obtained. One of these, 3-(2-ethylphenyl)-5-(3-methoxyphenyl)-s-triazole, DL 111 (36), was selected for detailed evaluation in various animal species. A synthetic scheme for the preparation of these compounds and preliminary structure-activity relationships are presented.
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