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hex-5-ynoic acid [2-(1H-imidazol-4-yl)ethyl]amide | 1027257-82-4

中文名称
——
中文别名
——
英文名称
hex-5-ynoic acid [2-(1H-imidazol-4-yl)ethyl]amide
英文别名
N-[2-(1H-imidazol-5-yl)ethyl]hex-5-ynamide
hex-5-ynoic acid [2-(1H-imidazol-4-yl)ethyl]amide化学式
CAS
1027257-82-4
化学式
C11H15N3O
mdl
——
分子量
205.26
InChiKey
CBBZQTQLNJCFDC-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:
    516.2±40.0 °C(Predicted)
  • 密度:
    1.124±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.5
  • 重原子数:
    15
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    57.8
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • Discovery of Chemoselective and Biocompatible Reactions Using a High-Throughput Immunoassay Screening
    作者:Sergii Kolodych、Evelia Rasolofonjatovo、Manon Chaumontet、Marie-Claire Nevers、Christophe Créminon、Frédéric Taran
    DOI:10.1002/anie.201305645
    日期:2013.11.11
    An immunoassay‐based method was used to screen numerous combinations of dipoles and dipolarophiles for their ability to undergo chemoselective and biocompatible [3+2] cycloaddition reactions. The approach fulfills most of the requirements of the click concept and led to the discovery of a copper‐catalyzed reaction that generates pyrazoles from sydnone and alkyne reagents.
    一种基于免疫分析的方法被用来筛选偶极子和亲偶极子的多种组合,使其具有化学选择性和生物相容性[3 + 2]环加成反应的能力。该方法满足了点击概念的大多数要求,并导致了催化反应的发现,该反应由亚砜和炔烃试剂生成吡唑
  • Method for screening process conditions of a chemical coupling reaction and kits therefor
    申请人:Taran Frederic
    公开号:US20070172905A1
    公开(公告)日:2007-07-26
    The present invention relates to a method of screening the operating conditions of a coupling reaction of at least two functional groups, and in particular of catalysts that are useful in this coupling reaction, and also to kits suitable for allowing this method to be carried out. Applications: fundamental and applied research, in particular in the areas of chemistry, agrofoods, pharmacy and environmental protection, for the development or optimization of synthesis reaction yields.
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