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| 929642-69-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
929642-69-3
化学式
C19H26O2Si
mdl
——
分子量
314.5
InChiKey
ZOLRHWVKCFNNIL-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):
    5.85
  • 重原子数:
    22.0
  • 可旋转键数:
    5.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    18.46
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    3-deuterocyclopentene-2-one-12,6-二叔丁基吡啶叔丁基二甲硅基三氟甲磺酸酯 作用下, 以 二氯甲烷 为溶剂, 以0.3283 g的产率得到naphthalen-2-ylmethyl 2-(3-oxocyclopentyl)-(2)H-ethanoate
    参考文献:
    名称:
    Synthesis of 2-Quinuclidonium by Eliminating Water:  Experimental Quantification of the High Basicity of Extremely Twisted Amides
    摘要:
    The chemical properties of an extremely twisted amide are examined quantitatively for the first time. The predicted high basicity of 2-quinuclidonium is confirmed experimentally by measuring the gas-phase proton affinity using the extended kinetic method. Fragmentation of this molecule further reveals that the lack of resonance stabilization weakens the amide bond. Furthermore, a new route for synthesizing 2-quinuclidonium by eliminating water is demonstrated in the gas phase.
    DOI:
    10.1021/ja067703m
  • 作为产物:
    描述:
    2-萘甲醇偶氮二甲酸二异丙酯三苯基膦lithium diisopropyl amide 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 0.25h, 生成
    参考文献:
    名称:
    Synthesis of 2-Quinuclidonium by Eliminating Water:  Experimental Quantification of the High Basicity of Extremely Twisted Amides
    摘要:
    The chemical properties of an extremely twisted amide are examined quantitatively for the first time. The predicted high basicity of 2-quinuclidonium is confirmed experimentally by measuring the gas-phase proton affinity using the extended kinetic method. Fragmentation of this molecule further reveals that the lack of resonance stabilization weakens the amide bond. Furthermore, a new route for synthesizing 2-quinuclidonium by eliminating water is demonstrated in the gas phase.
    DOI:
    10.1021/ja067703m
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