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5-chloro-3-methoxycatechol | 4085-06-7

中文名称
——
中文别名
——
英文名称
5-chloro-3-methoxycatechol
英文别名
5-Chlor-pyrogallol-1-methylether;5-Chlor-3-methoxy-brenzcatechin;5-Chloro-3-methoxycatechol;5-chloro-3-methoxybenzene-1,2-diol
5-chloro-3-methoxycatechol化学式
CAS
4085-06-7
化学式
C7H7ClO3
mdl
——
分子量
174.584
InChiKey
BZBCKNGIVAGPGS-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):
    0.8
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    49.7
  • 氢给体数:
    2
  • 氢受体数:
    3

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
  • 下游产品
    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

  • Preparation and properties of chloro-3-methoxycatechols-components of pulp bleaching effluents
    作者:Terrence J. Smith、Ross H. Wearne、Adrian F.A. Wallis
    DOI:10.1016/0045-6535(94)90008-6
    日期:1994.3
    The preparation and properties are given for the seven chlorinated 3-methoxycatechols, several of which have been reported as components of pulp bleaching effluents. The 4- and 6-substituted compounds and the trichloro-3-methoxycatechol were obtained by direct chlorination of the parent catechol or its diacetate. The 5-substituted compound was prepared by the known addition of hydrochloric acid to 3-methoxy-ortho-benzoquinone, and further chlorination gave the 4,5- and 5,6-dichloro isomers. The diacetates of all seven compounds were separated by gas chromatography. Electron impact mass spectra and H-1 and C-13 NMR data for the diacetates are given.
  • Horner,L.; Goewecke,S., Chemische Berichte, 1961, vol. 94, p. 1267 - 1276
    作者:Horner,L.、Goewecke,S.
    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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