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2-O-methyl 3-O-(2-trimethylsilylethyl) 4-methyl-1H-pyrrole-2,3-dicarboxylate | 851590-92-6

中文名称
——
中文别名
——
英文名称
2-O-methyl 3-O-(2-trimethylsilylethyl) 4-methyl-1H-pyrrole-2,3-dicarboxylate
英文别名
——
2-O-methyl 3-O-(2-trimethylsilylethyl) 4-methyl-1H-pyrrole-2,3-dicarboxylate化学式
CAS
851590-92-6
化学式
C13H21NO4Si
mdl
——
分子量
283.4
InChiKey
UKLOPSSHYTZDIR-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:
    384.3±42.0 °C(Predicted)
  • 密度:
    1.083±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    19
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    68.4
  • 氢给体数:
    1
  • 氢受体数:
    4

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:
    参考文献:
    名称:
    Phosphine-catalyzed regioselective heteroaromatization between activated alkynes and isocyanides leading to pyrroles
    摘要:
    The organophosphine catalyzed reaction of activated alkynes with isocyanides produces the corresponding heteroaromatization products, pyrroles, regioselectively in good yields. The reaction proceeds most probably through the 1,4-addition of the nucleophilic phosphine catalyst to the alkynes, followed by a [3+2] cycloaddition between the resulting alkenyl phosphine intermediates and a carbanion derived from the isocyanides. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2005.02.104
  • 作为产物:
    参考文献:
    名称:
    Phosphine-catalyzed regioselective heteroaromatization between activated alkynes and isocyanides leading to pyrroles
    摘要:
    The organophosphine catalyzed reaction of activated alkynes with isocyanides produces the corresponding heteroaromatization products, pyrroles, regioselectively in good yields. The reaction proceeds most probably through the 1,4-addition of the nucleophilic phosphine catalyst to the alkynes, followed by a [3+2] cycloaddition between the resulting alkenyl phosphine intermediates and a carbanion derived from the isocyanides. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2005.02.104
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