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(S)-5-Hydroxy-nonanoic acid ((S)-1-naphthalen-1-yl-ethyl)-amide | 483287-65-6

中文名称
——
中文别名
——
英文名称
(S)-5-Hydroxy-nonanoic acid ((S)-1-naphthalen-1-yl-ethyl)-amide
英文别名
——
(S)-5-Hydroxy-nonanoic acid ((S)-1-naphthalen-1-yl-ethyl)-amide化学式
CAS
483287-65-6
化学式
C21H29NO2
mdl
——
分子量
327.467
InChiKey
PUUSNAVBUQGQJQ-WMZOPIPTSA-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:
    544.4±43.0 °C(Predicted)
  • 密度:
    1.058±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.74
  • 重原子数:
    24.0
  • 可旋转键数:
    9.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    49.33
  • 氢给体数:
    2.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Optical Resolution of Fragrant Lactones
    摘要:
    Optical resolution of six chiral fragrant lactones (delta-jasmine lactone, massoia lactone, tuberolactone, pentynyllactone, delta-decalactone, and gamma-nonalactone) was investigated by means of either the diastereomeric salt formation method or the diastereomeric amide formation method. Using these procedures, we obtained each enantiomer from five of the six lactones, except for massoia lactone. All five lactones were obtained in a good yield and with high optical purity. Sensoric characteristics on both enantiomers and racemic modification of four lactones are given.
    DOI:
    10.3987/com-99-s149
  • 作为产物:
    描述:
    (S)-(-)-1-(1-萘基)乙胺γ-壬内酯甲苯 为溶剂, 以30.2%的产率得到(S)-5-Hydroxy-nonanoic acid ((S)-1-naphthalen-1-yl-ethyl)-amide
    参考文献:
    名称:
    Optical Resolution of Fragrant Lactones
    摘要:
    Optical resolution of six chiral fragrant lactones (delta-jasmine lactone, massoia lactone, tuberolactone, pentynyllactone, delta-decalactone, and gamma-nonalactone) was investigated by means of either the diastereomeric salt formation method or the diastereomeric amide formation method. Using these procedures, we obtained each enantiomer from five of the six lactones, except for massoia lactone. All five lactones were obtained in a good yield and with high optical purity. Sensoric characteristics on both enantiomers and racemic modification of four lactones are given.
    DOI:
    10.3987/com-99-s149
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