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6-acetoxy-1-naphthoic chloride | 832146-39-1

中文名称
——
中文别名
——
英文名称
6-acetoxy-1-naphthoic chloride
英文别名
6-acetoxy-[1]naphthoyl chloride;6-Acetoxy-naphthoesaeure-(1)-chlorid;6-Acetoxy-[1]naphthoylchlorid
6-acetoxy-1-naphthoic chloride化学式
CAS
832146-39-1
化学式
C13H9ClO3
mdl
——
分子量
248.666
InChiKey
ZCFBLRSDMCDUPY-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):
    3.14
  • 重原子数:
    17.0
  • 可旋转键数:
    2.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    43.37
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

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

  • Synthesis and Curing Behaviors of Cross-Linkable Polynaphthols from Renewable Resources:  Preparation of Artificial Urushi
    作者:Takashi Tsujimoto、Hiroshi Uyama、Shiro Kobayashi
    DOI:10.1021/ma035271j
    日期:2004.3.1
    This paper describes the synthesis and curing of cross-linkable polynaphthols from renewable resources. Naphthol monomers bearing an unsaturated group from renewable triglyceride oils were designed and oxidatively polymerized to produce new cross-linkable precursor polymers. The monomers were prepared by acylation of hydroxynaphthoic acids with unsaturated alcohols, obtained by reduction of natural oils. The oxidative polymerization was carried out by Fe-salen catalyst to give soluble polynaphthols. NMR analysis showed that the naphthol moiety was chemoselectively reacted during the polymerization, yielding the polymers possessing the unsaturated group in the side chain. The resulting polymers were readily cured by thermal treatment or cobalt naphthenate catalyst to give the cross-linked film ("artificial urushi") with high hardness and gloss surface.
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