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2-(2-fluorophenoxy)propanoyl chloride | 904702-97-2

中文名称
——
中文别名
——
英文名称
2-(2-fluorophenoxy)propanoyl chloride
英文别名
——
2-(2-fluorophenoxy)propanoyl chloride化学式
CAS
904702-97-2
化学式
C9H8ClFO2
mdl
——
分子量
202.613
InChiKey
HLFFXTZPFVSMKY-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):
    2.36
  • 重原子数:
    13.0
  • 可旋转键数:
    3.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    26.3
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Design, synthesis and structure–activity relationship studies of novel phenoxyacetamide-based free fatty acid receptor 1 agonists for the treatment of type 2 diabetes
    作者:Zheng Li、Xuekun Wang、Xue Xu、Jianyong Yang、Qianqian Qiu、Hao Qiang、Wenlong Huang、Hai Qian
    DOI:10.1016/j.bmc.2015.09.010
    日期:2015.10
    The free fatty acid receptor 1 (FFA1) has attracted extensive attention as a novel antidiabetic target in the last decade. Several FFA1 agonists reported in the literature have been suffered from relatively high molecular weight and lipophilicity. We have previously reported the FFA1 agonist 1. Based on the common amide structural characteristic of SAR1 and NIH screened compound, we here describe the continued structure-activity exploration to decrease the molecular weight and lipophilicity of the compound 1 series by converting various amide linkers. All of these efforts lead to the discovery of the preferable lead compound 18, a compound with considerable agonistic activity, high LE and LLE values, lower lipophilicity than previously reported agonists, and appreciable efficacy on glucose tolerance in both normal and type 2 diabetic mice. (c) 2015 Published by Elsevier Ltd.
  • Synthesis and Herbicidal Activity of α-[2-(Fluoro-Substituted Phenoxy)Propionyloxy] Alkyl Phosphonates
    作者:Yan-Jun Li、Hong-Wu He
    DOI:10.1080/10426500701807566
    日期:2008.1.14
    Eight of novel fluoro-substituted phosphonate derivatives were synthesized and the preliminary bioassay indicated that these compounds exhibited herbicidal activities.
    合成了八种新型氟取代膦酸酯衍生物,初步生物测定表明这些化合物具有除草活性。
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