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1,2,3-trihydroxy-4,6-dichlorobenzene | 87441-03-0

中文名称
——
中文别名
——
英文名称
1,2,3-trihydroxy-4,6-dichlorobenzene
英文别名
4,6-dichloropyrogallol;4,6-dichloro-pyrogallol;4,6-Dichlor-pyrogallol;4.6-Dichlor-1.2.3-trihydroxy-benzol;Dichloropyrogallol;4,6-dichlorobenzene-1,2,3-triol
1,2,3-trihydroxy-4,6-dichlorobenzene化学式
CAS
87441-03-0
化学式
C6H4Cl2O3
mdl
——
分子量
195.002
InChiKey
SLTWBTVSKQNVHF-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:
    310.8±37.0 °C(Predicted)
  • 密度:
    1.795±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    60.7
  • 氢给体数:
    3
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1,2,3-trihydroxy-4,6-dichlorobenzene乙酸酐吡啶 作用下, 生成 4,6-dichloropyrogallol triacetate
    参考文献:
    名称:
    Preparation of chlorosyringols and chloropyrogallols-components of pulp bleaching effluents
    摘要:
    The preparation and properties of chlorosyringols and chloropyrogallols, components of pulp bleaching effluents, and their acetates are given. The compounds are obtained mainly by direct chlorination of both phenols or of syringol acetate with various chlorinating reagents. 5-Chloropyrogallol and 4,5-dichloropyrogallol were the products of demethylation of 5-chloro-3-methoxycatechol acetate and 4,5-dichloro-3-methoxycatechol acetate, respectively. The acetates of all ten chloro compounds were separated by gas chromatography. Electron impact mass spectra and H-1 and C-13 NMR data for the acetates are given.
    DOI:
    10.1016/0045-6535(94)90009-4
  • 作为产物:
    描述:
    邻苯三酚磺酰氯 作用下, 以 乙醚 为溶剂, 反应 1.0h, 以1.30 g的产率得到1,2,3-trihydroxy-4,6-dichlorobenzene
    参考文献:
    名称:
    Preparation of chlorosyringols and chloropyrogallols-components of pulp bleaching effluents
    摘要:
    The preparation and properties of chlorosyringols and chloropyrogallols, components of pulp bleaching effluents, and their acetates are given. The compounds are obtained mainly by direct chlorination of both phenols or of syringol acetate with various chlorinating reagents. 5-Chloropyrogallol and 4,5-dichloropyrogallol were the products of demethylation of 5-chloro-3-methoxycatechol acetate and 4,5-dichloro-3-methoxycatechol acetate, respectively. The acetates of all ten chloro compounds were separated by gas chromatography. Electron impact mass spectra and H-1 and C-13 NMR data for the acetates are given.
    DOI:
    10.1016/0045-6535(94)90009-4
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文献信息

  • Halogenation of Pyrogallol Trimethyl Ether and Similar Systems<sup>1a</sup>
    作者:DVORA FRIEDMAN、DAVID GINSBURG
    DOI:10.1021/jo01095a005
    日期:1958.1
  • Peratoner, Gazzetta Chimica Italiana, 1898, vol. 28 I, p. 222
    作者:Peratoner
    DOI:——
    日期:——
  • Preparation of chlorosyringols and chloropyrogallols-components of pulp bleaching effluents
    作者:Terrence J. Smith、Ross H. Wearne、Adrian F.A. Wallis
    DOI:10.1016/0045-6535(94)90009-4
    日期:1994.3
    The preparation and properties of chlorosyringols and chloropyrogallols, components of pulp bleaching effluents, and their acetates are given. The compounds are obtained mainly by direct chlorination of both phenols or of syringol acetate with various chlorinating reagents. 5-Chloropyrogallol and 4,5-dichloropyrogallol were the products of demethylation of 5-chloro-3-methoxycatechol acetate and 4,5-dichloro-3-methoxycatechol acetate, respectively. The acetates of all ten chloro compounds were separated by gas chromatography. Electron impact mass spectra and H-1 and C-13 NMR data for the acetates are given.
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