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anilino(2,5-dimethyl-1-phenyl-1H-pyrrol-3-yl)acetonitrile | 1260237-23-7

中文名称
——
中文别名
——
英文名称
anilino(2,5-dimethyl-1-phenyl-1H-pyrrol-3-yl)acetonitrile
英文别名
2-Anilino-2-(2,5-dimethyl-1-phenylpyrrol-3-yl)acetonitrile
anilino(2,5-dimethyl-1-phenyl-1H-pyrrol-3-yl)acetonitrile化学式
CAS
1260237-23-7
化学式
C20H19N3
mdl
——
分子量
301.391
InChiKey
NLDZKWLEKZDSBA-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):
    4.6
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    40.8
  • 氢给体数:
    1
  • 氢受体数:
    2

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:
    三甲基氰硅烷1-(2,5-二甲基-1-苯基-1H-吡咯-3-基)乙烷-1-酮苯胺 为溶剂, 反应 12.0h, 以92%的产率得到anilino(2,5-dimethyl-1-phenyl-1H-pyrrol-3-yl)acetonitrile
    参考文献:
    名称:
    Water-Mediated Strecker Reaction: An Efficient and Environmentally Friendly Approach for the Synthesis of α-Aminonitriles via a Three-Component Condensation
    摘要:
    The synthesis of -aminonitriles by a direct three component Strecker reaction has been achieved in water, which is found to be an inexpensive, non-toxic and eco-friendly reaction medium for the nucleophilic addition. This protocol is effective to a wide variety of substrates with different functional groups and does not require the use any other catalyst.
    DOI:
    10.1080/00397910903457381
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文献信息

  • Water-Mediated Strecker Reaction: An Efficient and Environmentally Friendly Approach for the Synthesis of <font>α</font>-Aminonitriles <i>via</i> a Three-Component Condensation
    作者:Samikannu Ramesh、Kulanthaivel Sivakumar、Chiradeep Panja、Pirama Nayagam Arunachalam、Appaswami Lalitha
    DOI:10.1080/00397910903457381
    日期:2010.11.3
    The synthesis of -aminonitriles by a direct three component Strecker reaction has been achieved in water, which is found to be an inexpensive, non-toxic and eco-friendly reaction medium for the nucleophilic addition. This protocol is effective to a wide variety of substrates with different functional groups and does not require the use any other catalyst.
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