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diethyl 4-decynoylmalonate | 1025737-69-2

中文名称
——
中文别名
——
英文名称
diethyl 4-decynoylmalonate
英文别名
——
diethyl 4-decynoylmalonate化学式
CAS
1025737-69-2
化学式
C17H28O4
mdl
——
分子量
296.407
InChiKey
IAJHRAHYTMLIAK-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:
    378.8±32.0 °C(predicted)
  • 密度:
    0.988±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.48
  • 重原子数:
    21.0
  • 可旋转键数:
    10.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.76
  • 拓扑面积:
    52.6
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    diethyl 4-decynoylmalonatelithium chloride 作用下, 以 二甲基亚砜 为溶剂, 反应 7.0h, 以76%的产率得到ethyl dodec-5-ynoate
    参考文献:
    名称:
    Synthesis and Stereochemistry-Activity Relationship of small Bacteriocin, an Autoinducer of the Symbiotic Nitrogen-Fixing Bacterium Rhizobium leguminosarum
    摘要:
    The four stereoisomers of small bacteriocin, an autoinducer of the symbiotic nitrogen-fixing bacterium Rhizobium leguminosarum, were synthesized via a versatile methodology for 3'-hydroxyacyl homoserine lactones based on the Nagao asymmetric aldol reaction. The synthetic isomers were much less effective at inhibiting the growth of R. leguminosarum RBL5523 than the natural isomer, showing the importance of stereochemistry for activity.
    DOI:
    10.1021/ol8005198
  • 作为产物:
    描述:
    1-碘-3-癸炔丙二酸二乙酯potassium carbonate 作用下, 以 N,N-二甲基甲酰胺丙酮 为溶剂, 反应 10.0h, 以100%的产率得到diethyl 4-decynoylmalonate
    参考文献:
    名称:
    Synthesis and Stereochemistry-Activity Relationship of small Bacteriocin, an Autoinducer of the Symbiotic Nitrogen-Fixing Bacterium Rhizobium leguminosarum
    摘要:
    The four stereoisomers of small bacteriocin, an autoinducer of the symbiotic nitrogen-fixing bacterium Rhizobium leguminosarum, were synthesized via a versatile methodology for 3'-hydroxyacyl homoserine lactones based on the Nagao asymmetric aldol reaction. The synthetic isomers were much less effective at inhibiting the growth of R. leguminosarum RBL5523 than the natural isomer, showing the importance of stereochemistry for activity.
    DOI:
    10.1021/ol8005198
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