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5-methyl-2-phenyloxazole-4-carboxylic acid diethylamide

中文名称
——
中文别名
——
英文名称
5-methyl-2-phenyloxazole-4-carboxylic acid diethylamide
英文别名
N,N-diethyl-5-methyl-2-phenyl-1,3-oxazole-4-carboxamide
5-methyl-2-phenyloxazole-4-carboxylic acid diethylamide化学式
CAS
——
化学式
C15H18N2O2
mdl
——
分子量
258.32
InChiKey
GVTZCRSPKQVUTA-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):
    2.9
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    46.3
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    N,N-二乙基乙酰乙酰胺苄胺碘化铵 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 8.0h, 以67%的产率得到5-methyl-2-phenyloxazole-4-carboxylic acid diethylamide
    参考文献:
    名称:
    在温和条件下用电化学方法促进β-二酮衍生物和苄胺合成多取代的恶唑†
    摘要:
    描述了由容易获得的β-二酮衍生物和苄胺有效地电化学合成多取代的恶唑的方法。该电化学程序不需要有害的氧化剂和过渡金属催化剂以及分子I 2添加剂。与传统的热化学方法相比,本发明的电化学方法更绿色,更有效。
    DOI:
    10.1039/c4ra03865g
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文献信息

  • Preparation of New Microgel Polymers and Their Application as Supports in Organic Synthesis
    作者:Carsten Spanka、Bruce Clapham、Kim D. Janda
    DOI:10.1021/jo016362m
    日期:2002.5.1
    A series of soluble microgel polymers have been synthesized using solution-phase polymerization reactions. In a systematic manner, several variables such as monomer concentration, cross-linker content, reaction solvent and reaction time were examined, and this provided an optimal polymer with both solubility and precipitation characteristics suitable for synthetic applications. Thus, a chemically functionalized microgel polymer was synthesized, and the utility of this polymer in the synthesis of a small array of oxazole compounds has been demonstrated. The advantage of the microgel polymers produced was that they exhibited solution viscosities lower than those of conventional linear polymers even at higher concentrations, and this was found to be beneficial for their precipitation properties. Compounds prepared using the described microgel polymer supports were obtained in similar yields and purity when compared with insoluble resins, and more importantly, the soluble polymer bound intermediates could be analyzed at each step using standard NMR techniques.
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