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1-isopropyl-2-cyano-1H-benzoimidazole | 1263902-87-9

中文名称
——
中文别名
——
英文名称
1-isopropyl-2-cyano-1H-benzoimidazole
英文别名
1-Propan-2-ylbenzimidazole-2-carbonitrile;1-propan-2-ylbenzimidazole-2-carbonitrile
1-isopropyl-2-cyano-1H-benzoimidazole化学式
CAS
1263902-87-9
化学式
C11H11N3
mdl
——
分子量
185.228
InChiKey
SZQIZHKCEDNGDI-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):
    2.2
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    41.6
  • 氢给体数:
    0
  • 氢受体数:
    2

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:
    1-isopropyl-2-cyano-1H-benzoimidazole 在 ammonium sulfide 、 三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 以47%的产率得到1-isopropyl-1H-benzoimidazole-2-carbothioic acid amide
    参考文献:
    名称:
    Synthesis and in vitro cytotoxic evaluation of some thiazolylbenzimidazole derivatives
    摘要:
    A novel kind of thiazolylbenzimidazole derivatives were designed and synthesized and evaluated for their antitumor activity against SMMC-7721 and A549 cell lines. Most compounds showed good antitumor activities, and compound lib displayed remarkable in vitro anticancer activity comparable to taxol. The preliminary structure-activity relationship of these benzimidazole derivatives was discussed based on the experimental data obtained. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.11.014
  • 作为产物:
    描述:
    sodium cyanide(9ci)-2-氯-1-(1-甲基乙基)-1H-苯并咪唑N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 以84%的产率得到1-isopropyl-2-cyano-1H-benzoimidazole
    参考文献:
    名称:
    Synthesis and in vitro cytotoxic evaluation of some thiazolylbenzimidazole derivatives
    摘要:
    A novel kind of thiazolylbenzimidazole derivatives were designed and synthesized and evaluated for their antitumor activity against SMMC-7721 and A549 cell lines. Most compounds showed good antitumor activities, and compound lib displayed remarkable in vitro anticancer activity comparable to taxol. The preliminary structure-activity relationship of these benzimidazole derivatives was discussed based on the experimental data obtained. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.11.014
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文献信息

  • Synthesis and in vitro cytotoxic evaluation of some thiazolylbenzimidazole derivatives
    作者:Yu Luo、Feng Xiao、Shijing Qian、Wei Lu、Bo Yang
    DOI:10.1016/j.ejmech.2010.11.014
    日期:2011.1
    A novel kind of thiazolylbenzimidazole derivatives were designed and synthesized and evaluated for their antitumor activity against SMMC-7721 and A549 cell lines. Most compounds showed good antitumor activities, and compound lib displayed remarkable in vitro anticancer activity comparable to taxol. The preliminary structure-activity relationship of these benzimidazole derivatives was discussed based on the experimental data obtained. (C) 2010 Elsevier Masson SAS. All rights reserved.
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