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1-(3,5-Dimethoxy-4-propyl-pyridin-2-yl)-ethanone | 910032-74-5

中文名称
——
中文别名
——
英文名称
1-(3,5-Dimethoxy-4-propyl-pyridin-2-yl)-ethanone
英文别名
——
1-(3,5-Dimethoxy-4-propyl-pyridin-2-yl)-ethanone化学式
CAS
910032-74-5
化学式
C12H17NO3
mdl
——
分子量
223.272
InChiKey
WMJYJFIXNAHIFI-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):
    2.25
  • 重原子数:
    16.0
  • 可旋转键数:
    5.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    48.42
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    1-(3,5-Dimethoxy-4-propyl-pyridin-2-yl)-ethanone三氯化铝potassium carbonate 、 potassium iodide 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 16.0h, 生成 Methyl 2-(4-(3-(6-acetyl-5-hydroxy-4-propylpyridin-3-yloxy)propoxy)phenoxy)acetate
    参考文献:
    名称:
    Studies towards the conception of new selective PPARβ/δ ligands
    摘要:
    In order to define new PPAR beta/delta ligands, SAR study on the selective PPAR beta/delta activator L-165,041 led to the identification of one key functional group for selective PPAR beta/delta activation. Further-more, taking advantage of SAR studies done elsewhere on the most selective PPAR beta/delta ligand GW501516, the conception of new ligands showing good affinity for PPAR beta/delta is reported. Finally, synthesis and biological evaluation of pyridine analogues have shown the benefical effect of the pyridine ring on the PPAR beta/ delta subtype selectivity. (c) 2006 Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmcl.2006.06.028
  • 作为产物:
    参考文献:
    名称:
    Studies towards the conception of new selective PPARβ/δ ligands
    摘要:
    In order to define new PPAR beta/delta ligands, SAR study on the selective PPAR beta/delta activator L-165,041 led to the identification of one key functional group for selective PPAR beta/delta activation. Further-more, taking advantage of SAR studies done elsewhere on the most selective PPAR beta/delta ligand GW501516, the conception of new ligands showing good affinity for PPAR beta/delta is reported. Finally, synthesis and biological evaluation of pyridine analogues have shown the benefical effect of the pyridine ring on the PPAR beta/ delta subtype selectivity. (c) 2006 Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmcl.2006.06.028
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