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1,4-benzoquinone-N-bromoimine | 64693-23-8

中文名称
——
中文别名
——
英文名称
1,4-benzoquinone-N-bromoimine
英文别名
[1,4]benzoquinone-mono-bromoimine;[1,4]Benzochinon-mono-bromimin;2,5-Cyclohexadien-1-one, 4-bromoimino-;4-bromoiminocyclohexa-2,5-dien-1-one
1,4-benzoquinone-N-bromoimine化学式
CAS
64693-23-8
化学式
C6H4BrNO
mdl
——
分子量
186.008
InChiKey
PZZRNAITVRJAKV-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):
    1.1
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    29.4
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:863d13f61ebf1b667cd81f8e917863cd
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反应信息

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文献信息

  • Burmistrow; Suikowa, Zhurnal Obshchei Khimii, 1950, vol. 20, p. 1852,1855; engl. Ausg. S. 1917, 1919
    作者:Burmistrow、Suikowa
    DOI:——
    日期:——
  • Nitrogen analogs of 1,4-benzoquinones. Activities against the ascitic sarcoma 180 of mice
    作者:Ernest M. Hodnett、Gopalakrishnan Prakash、Jafargholi Amirmoazzami
    DOI:10.1021/jm00199a003
    日期:1978.1
    Compounds having the basic structure N-(R)-substituted ring-substituted 4-iminocyclohexadienone have been synthesized and tested as antitumor agents against the ascitic sarcoma 180 tumor in Swiss mice. Among these compounds, the dimethylindoanilines [R = 4-(CH3)2NC6H4] are most stable in water at pH 7.0 and at 25 degrees C, the oximes (R = oh) are less stable, and the N-halo compounds (R = Br and Cl) are least stable. The N-halo derivatives have the highest redox potentials under the conditions used, the greatest effect against ascitic sarcoma 180 in Swiss mice, and the greatest acute toxicity when injected ip in the Swiss mice. Discriminant analysis of the results indicates that substituents with positive values of F and negative values of pi increase the antitumor activities, whereas those with positive values of sigma and R should lower the toxicity. The redox potential, a molecular parameter, is the best single variable for discriminating between the groups based on antitumor activities.
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