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1,2-bis(11H-indeno[2,1-b]quinoxalin-11-ylidene)hydrazine | 1544692-24-1

中文名称
——
中文别名
——
英文名称
1,2-bis(11H-indeno[2,1-b]quinoxalin-11-ylidene)hydrazine
英文别名
1,2-di(11H-indeno[2,1-b]quinoxalin-11-ylidene)hydrazine
1,2-bis(11H-indeno[2,1-b]quinoxalin-11-ylidene)hydrazine化学式
CAS
1544692-24-1
化学式
C30H16N6
mdl
——
分子量
460.497
InChiKey
CWZYIYACFCLFSM-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):
    5.82
  • 重原子数:
    36.0
  • 可旋转键数:
    1.0
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    76.28
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

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

反应信息

  • 作为产物:
    描述:
    11H-茚并[1,2-b]喹喔啉-11-酮2-碘苯甲酰肼溶剂黄146 作用下, 以 乙醇 为溶剂, 以25%的产率得到1,2-bis(11H-indeno[2,1-b]quinoxalin-11-ylidene)hydrazine
    参考文献:
    名称:
    Synthesis of novel indenoquinoxaline derivatives as potent α-glucosidase inhibitors
    摘要:
    A series of new N-(11H-Indeno[1,2-b]quinoxalin-11-ylidene)benzohydrazide derivatives (3a-3p) were synthesized and evaluated for their alpha-glucosidase inhibitory activity. The synthesized compounds 3d, 3f, 3g, 3k, 3n, 3p and 4 showed significant alpha-glucosidase inhibitory activity as compared to acrabose, a standard drug used to treat type II diabetes. Structures of the synthesized compounds were determined by using FT-IR, H-1 NMR, C-13 NMR, mass spectrometry and elemental analysis techniques. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.12.024
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文献信息

  • Synthesis of novel indenoquinoxaline derivatives as potent α-glucosidase inhibitors
    作者:Madiha Sahar Khan、Munawar Ali Munawar、Mohammad Ashraf、Umber Alam、Athar Ata、Abdullah Mohamed Asiri、Samina Kousar、Misbahul Ain Khan
    DOI:10.1016/j.bmc.2013.12.024
    日期:2014.2
    A series of new N-(11H-Indeno[1,2-b]quinoxalin-11-ylidene)benzohydrazide derivatives (3a-3p) were synthesized and evaluated for their alpha-glucosidase inhibitory activity. The synthesized compounds 3d, 3f, 3g, 3k, 3n, 3p and 4 showed significant alpha-glucosidase inhibitory activity as compared to acrabose, a standard drug used to treat type II diabetes. Structures of the synthesized compounds were determined by using FT-IR, H-1 NMR, C-13 NMR, mass spectrometry and elemental analysis techniques. (C) 2013 Elsevier Ltd. All rights reserved.
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