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4-amino-3-acetylenetrimethylsililisoquinoline | 271784-16-8

中文名称
——
中文别名
——
英文名称
4-amino-3-acetylenetrimethylsililisoquinoline
英文别名
4-amino-3-trimethylsilylethynylisoquinoline;3-(2-Trimethylsilylethynyl)isoquinolin-4-amine
4-amino-3-acetylenetrimethylsililisoquinoline化学式
CAS
271784-16-8
化学式
C14H16N2Si
mdl
——
分子量
240.38
InChiKey
OGPMIKANGCHHEV-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):
    3.05
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    38.9
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    4-amino-3-acetylenetrimethylsililisoquinoline 在 sodium amide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 16.0h, 以78%的产率得到1H-pyrrolo[3,2-c]isoquinoline
    参考文献:
    名称:
    Efficient Asymmetric Synthesis of Tryptophan Analogues Having Useful Photophysical Properties
    摘要:
    Two new fluorescent probes of protein structure and dynamics have been prepared by concise asymmetric syntheses using the Schollkopf chiral auxiliary. The site-specific incorporation of one probe into dihydrofolate reductase is reported. The utility of these tryptophan derivatives lies in their absorption and emission maxima which differ from those of tryptophan, as well as in their large Stokes shifts and high molar absorptivities.
    DOI:
    10.1021/ol403429e
  • 作为产物:
    描述:
    4-溴异喹啉 在 bis-triphenylphosphine-palladium(II) chloride 、 ammonium hydroxidecopper(l) iodide 、 silver sulfate 、 三乙胺copper(l) chloride 作用下, 以 四氢呋喃乙醇 为溶剂, 反应 48.0h, 生成 4-amino-3-acetylenetrimethylsililisoquinoline
    参考文献:
    名称:
    Efficient Asymmetric Synthesis of Tryptophan Analogues Having Useful Photophysical Properties
    摘要:
    Two new fluorescent probes of protein structure and dynamics have been prepared by concise asymmetric syntheses using the Schollkopf chiral auxiliary. The site-specific incorporation of one probe into dihydrofolate reductase is reported. The utility of these tryptophan derivatives lies in their absorption and emission maxima which differ from those of tryptophan, as well as in their large Stokes shifts and high molar absorptivities.
    DOI:
    10.1021/ol403429e
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文献信息

  • Briere, Jean-Francois; Dupas, Georges; Queguiner, Guy, Heterocycles, 2000, vol. 52, # 3, p. 1371 - 1383
    作者:Briere, Jean-Francois、Dupas, Georges、Queguiner, Guy、Bourguignon, Jean
    DOI:——
    日期:——
  • Efficient Asymmetric Synthesis of Tryptophan Analogues Having Useful Photophysical Properties
    作者:Poulami Talukder、Shengxi Chen、Pablo M. Arce、Sidney M. Hecht
    DOI:10.1021/ol403429e
    日期:2014.1.17
    Two new fluorescent probes of protein structure and dynamics have been prepared by concise asymmetric syntheses using the Schollkopf chiral auxiliary. The site-specific incorporation of one probe into dihydrofolate reductase is reported. The utility of these tryptophan derivatives lies in their absorption and emission maxima which differ from those of tryptophan, as well as in their large Stokes shifts and high molar absorptivities.
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