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N-(1,3-dimethyl-4-nitro-2,6-dioxopyrimidin-5-yl)formamide | 624734-82-3

中文名称
——
中文别名
——
英文名称
N-(1,3-dimethyl-4-nitro-2,6-dioxopyrimidin-5-yl)formamide
英文别名
——
N-(1,3-dimethyl-4-nitro-2,6-dioxopyrimidin-5-yl)formamide化学式
CAS
624734-82-3
化学式
C7H8N4O5
mdl
——
分子量
228.164
InChiKey
SNXOWRQWXNGXMZ-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

  • 沸点:
    356.0±52.0 °C(Predicted)
  • 密度:
    1.58±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    116
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    N-(1,3-dimethyl-4-nitro-2,6-dioxopyrimidin-5-yl)formamide铁粉 、 sodium hydride 、 溶剂黄146 作用下, 以 二甲基亚砜 为溶剂, 反应 1.25h, 生成 咖啡因
    参考文献:
    名称:
    A Novel Method of Caffeine Synthesis from Uracil
    摘要:
    An inexpensive and novel method of caffeine synthesis starting from uracil in six simple steps is described. Uracil 1 is first converted to I, 3-dimethyluracil 2, followed by nitration, reduction, and cyclization to theophylline and finally methylation of theophylline forms caffeine.
    DOI:
    10.1081/scc-120023986
  • 作为产物:
    参考文献:
    名称:
    A Novel Method of Caffeine Synthesis from Uracil
    摘要:
    An inexpensive and novel method of caffeine synthesis starting from uracil in six simple steps is described. Uracil 1 is first converted to I, 3-dimethyluracil 2, followed by nitration, reduction, and cyclization to theophylline and finally methylation of theophylline forms caffeine.
    DOI:
    10.1081/scc-120023986
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文献信息

  • A Novel Method of Caffeine Synthesis from Uracil
    作者:Zajac, Matthew A.、Zakrzewski, Anthony G.、Kowal, Mark G.、Narayan, Saraswathi
    DOI:10.1081/scc-120023986
    日期:2003.9
    An inexpensive and novel method of caffeine synthesis starting from uracil in six simple steps is described. Uracil 1 is first converted to I, 3-dimethyluracil 2, followed by nitration, reduction, and cyclization to theophylline and finally methylation of theophylline forms caffeine.
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