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2,8-二甲基-4-肼基喹啉 | 49612-06-8

中文名称
2,8-二甲基-4-肼基喹啉
中文别名
——
英文名称
4-hydrazino-2,8-dimethylquinoline
英文别名
(2,8-dimethyl-[4]quinolyl)-hydrazine;(2,8-Dimethyl-[4]chinolyl)-hydrazin;(2,8-dimethylquinolin-4-yl)hydrazine
2,8-二甲基-4-肼基喹啉化学式
CAS
49612-06-8
化学式
C11H13N3
mdl
——
分子量
187.244
InChiKey
XDMSDOXCZHKTDD-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

物化性质

  • 熔点:
    199 °C
  • 沸点:
    370.5±37.0 °C(Predicted)
  • 密度:
    1.200±0.06 g/cm3(Predicted)

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:
    0.18
  • 拓扑面积:
    50.9
  • 氢给体数:
    2
  • 氢受体数:
    3

SDS

SDS:1e835a053ca12416898f575f3e4712c6
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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

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文献信息

  • N 1-{4-[(10S)-Dihydroartemisinin-10-oxyl]}phenylmethylene-N 2-(2-methylquinoline-4-yl)hydrazine derivatives as antiplasmodial falcipain-2 inhibitors
    作者:Wei Luo、Wei-Qiang Lu、Kun-Qiang Cui、Yang Liu、Jian Wang、Chun Guo
    DOI:10.1007/s00044-011-9854-3
    日期:2012.10
    A series of N (1)-4-[(10S)-dihydroartemisinin-10-oxyl]}phenylmethylene-N (2)-(2-methylquinoline-4-yl) hydrazine derivatives 9a-9n possessing 4-quinolylhydrazone and artemisinin cores were herein synthesized and evaluated for their activities against cysteine protease falcipain-2 of Plasmodium falciparum. The structures were clearly confirmed by elemental analysis, H-1 NMR, and mass spectra. The pharmacological results indicated that all compounds showed excellent activity against recombinant falcipain-2 (IC50 = 0.15-2.28 mu M). The best one of this series was compound 9d (IC50 = 0.15 mu M). The molecular docking results showed that the compound 9d made close contact with the key active site of cysteine protease falcipain-2.
  • Pellerano; Savini; Brizzi, Farmaco, Edizione Scientifica, 1985, vol. 40, # 7, p. 486 - 492
    作者:Pellerano、Savini、Brizzi
    DOI:——
    日期:——
  • Synthesis and some transformations of 6(8)-substituted 4-hydrazino-2-methylquinolines
    作者:A. A. Avetisyan、I. L. Aleksanyan、L. P. Ambartsumyan
    DOI:10.1134/s107042801003022x
    日期:2010.3
    6(8)-Substituted 4-hydrazino-2-methylquinolines were synthesized by reaction of the corresponding 4-chloro-2-methylquinolines with hydrazine hydrate. Reactions of the title compounds with ethyl acetoacetate and acetone gave 2,4-dimethyl-1H-pyrrolo[3,2-c]quinolines and 4-(5-ethoxy-3-methyl-1H-pyrazol-1-yl)-2-methylquinolines.
  • PELLERANO, C.;SAVINI, L., FARMACO. ED. SCI., 1984, 39, N 8, 681-685
    作者:PELLERANO, C.、SAVINI, L.
    DOI:——
    日期:——
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