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8-氟-2(1H)-喹喔啉酮 | 55687-17-7

中文名称
8-氟-2(1H)-喹喔啉酮
中文别名
——
英文名称
8-fluoro-2(1H)-quinoxalinone
英文别名
8-fluoro-1H-quinoxalin-2-one;8-fluoroquinoxalin-2(1H)-one;8-Fluoroquinoxalin-2-ol;8-fluoro-1H-quinoxalin-2-one
8-氟-2(1H)-喹喔啉酮化学式
CAS
55687-17-7
化学式
C8H5FN2O
mdl
——
分子量
164.139
InChiKey
ZHHVHNXHZINQDX-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):
    0.8
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    41.5
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 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:
    8-氟-2(1H)-喹喔啉酮三氯氧磷 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 1.5h, 生成 2-氯-8-氟喹喔啉
    参考文献:
    名称:
    Piperazinylquinoxalines with central serotoninmimetic activity
    摘要:
    Regioselective syntheses of substituted 2-chloroquinoxalines and derived 2-(1-piperazinyl)quinoxalines are described. Selectivity in regards to serotonin reuptake blocking and serotoninmimetic activities of the piperazinylquinoxalines is reported. In general, introduction of a 6-substituent into the piperazinylquinoxaline enhanced serotonin reuptake blocking activity and diminished serotoninmimetic activity. Unsubstituted and 3-hydroxypiperazinylquinoxalines had primarily serotoninmimetic activity.
    DOI:
    10.1021/jm00133a019
  • 作为产物:
    描述:
    2,6-二氟硝基苯盐酸sodium hydroxidetin双氧水 作用下, 以 乙醇 为溶剂, 反应 21.75h, 生成 8-氟-2(1H)-喹喔啉酮
    参考文献:
    名称:
    Piperazinylquinoxalines with central serotoninmimetic activity
    摘要:
    Regioselective syntheses of substituted 2-chloroquinoxalines and derived 2-(1-piperazinyl)quinoxalines are described. Selectivity in regards to serotonin reuptake blocking and serotoninmimetic activities of the piperazinylquinoxalines is reported. In general, introduction of a 6-substituent into the piperazinylquinoxaline enhanced serotonin reuptake blocking activity and diminished serotoninmimetic activity. Unsubstituted and 3-hydroxypiperazinylquinoxalines had primarily serotoninmimetic activity.
    DOI:
    10.1021/jm00133a019
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文献信息

  • LUMMA W. C. JR.; HARTMAN R. D.; SAARI W. S.; ENGELHARDT E. L.; LOTTI V. J+, J. MED. CHEM., 1981, 24, NO 1, 93-101
    作者:LUMMA W. C. JR.、 HARTMAN R. D.、 SAARI W. S.、 ENGELHARDT E. L.、 LOTTI V. J+
    DOI:——
    日期:——
  • Piperazinylquinoxalines with central serotoninmimetic activity
    作者:William C. Lumma、Richard D. Hartman、Walfred S. Saari、Edward L. Engelhardt、Victor J. Lotti、Clement A. Stone
    DOI:10.1021/jm00133a019
    日期:1981.1
    Regioselective syntheses of substituted 2-chloroquinoxalines and derived 2-(1-piperazinyl)quinoxalines are described. Selectivity in regards to serotonin reuptake blocking and serotoninmimetic activities of the piperazinylquinoxalines is reported. In general, introduction of a 6-substituent into the piperazinylquinoxaline enhanced serotonin reuptake blocking activity and diminished serotoninmimetic activity. Unsubstituted and 3-hydroxypiperazinylquinoxalines had primarily serotoninmimetic activity.
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