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5-(6-fluoro-4-oxo-4H-chromen-3-ylmethylene)-pyrimidine-2,4,6-trione

中文名称
——
中文别名
——
英文名称
5-(6-fluoro-4-oxo-4H-chromen-3-ylmethylene)-pyrimidine-2,4,6-trione
英文别名
Pyrimidine-2,4,6-trione, hexahydro-5-(6-fluoro-4-oxo-4H-chromen-3-ylmethylene)-;5-[(6-fluoro-4-oxochromen-3-yl)methylidene]-1,3-diazinane-2,4,6-trione
5-(6-fluoro-4-oxo-4H-chromen-3-ylmethylene)-pyrimidine-2,4,6-trione化学式
CAS
——
化学式
C14H7FN2O5
mdl
——
分子量
302.218
InChiKey
PFCBZDYBKJAILL-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):
    0.7
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    102
  • 氢给体数:
    2
  • 氢受体数:
    6

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:
    巴比妥酸6-氟色同-3-甲醛D(+)-10-樟脑磺酸 作用下, 以 乙醇 为溶剂, 反应 0.33h, 以76%的产率得到5-(6-fluoro-4-oxo-4H-chromen-3-ylmethylene)-pyrimidine-2,4,6-trione
    参考文献:
    名称:
    (±)-Camphor-10-sulfonic acid as recyclable and efficient catalyst for the synthesis of some novel coumarin derivatives
    摘要:
    A highly competent-diversity oriented synthesis of coumarin core derivatives using a Knoevenagel condensation followed by Michael addition and subsequent cyclization in the presence of (+/-)-camphor-10-sulfonic acid in a water/ethanol (1:1) solvent system is depicted. Furthermore, easy workup procedures with good yield, rapid reactions with high atom economy, and catalyst recyclability are the fascinating features of the procedure.
    DOI:
    10.1080/00397911.2015.1121281
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文献信息

  • (±)-Camphor-10-sulfonic acid as recyclable and efficient catalyst for the synthesis of some novel coumarin derivatives
    作者:Digambar Kumbhar、Reshma Patil、Dayanand Patil、Ajinkya Patravale、Dattatray Chandam、Sunetra Jadhav、Madhukar Deshmukh
    DOI:10.1080/00397911.2015.1121281
    日期:2016.1.2
    A highly competent-diversity oriented synthesis of coumarin core derivatives using a Knoevenagel condensation followed by Michael addition and subsequent cyclization in the presence of (+/-)-camphor-10-sulfonic acid in a water/ethanol (1:1) solvent system is depicted. Furthermore, easy workup procedures with good yield, rapid reactions with high atom economy, and catalyst recyclability are the fascinating features of the procedure.
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