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4-甲基-5-磺酰基-苯-1,2-二醇 | 27320-24-7

中文名称
4-甲基-5-磺酰基-苯-1,2-二醇
中文别名
——
英文名称
2-Mercapto-4,5-dihydroxy-toluol
英文别名
Pyrocatechol, 4-mercapto-5-methyl-;4-methyl-5-sulfanylbenzene-1,2-diol
4-甲基-5-磺酰基-苯-1,2-二醇化学式
CAS
27320-24-7
化学式
C7H8O2S
mdl
MFCD24390925
分子量
156.205
InChiKey
NSHDEDGWZUKSDC-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):
    1.7
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.142
  • 拓扑面积:
    41.5
  • 氢给体数:
    3
  • 氢受体数:
    3

SDS

SDS:6d14c70085a21bf3b55bafe8100f7346
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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

  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis, redox characteristics, and in vitro norepinephrine uptake inhibiting properties of 2-(2-mercapto-4,5-dihydroxyphenyl)ethylamine (6-mercaptodopamine)
    摘要:
    In an attempt to further characterize the structural features of 6-hydroxydopamine analogues that are associated with in vivo neuronal degeneration, the synthesis of 6-mercaptodopamine was undertaken. Although reaction conditions leading to the 1,4 addition of thiols to the model quinone 4-methyl-o-benzoquinone were achieved, attempts to obtain 6-thiolated dopamine analogues by this route failed. The synthesis of 6-mercaptodopamine was achieved by the regioselective thiocyanation of O,O-dimethyldopamine, followed by bis-O-demethylation and reductive cleavage of the S-cyano group. Unlike 6-hydroxydopamine, 6-mercaptodopamine was resistant to autoxidation at pH 7.4. Cyclic voltammometric analysis, however, indicated that electrochemically generated oxidation species of 6-mercaptodopamine are unstable and undergo spontaneous reaction, presumably intramolecular cyclization. In vivo tests revealed that 6-mercaptodopamine inhibits the uptake of tritium-labeled norepinephrine by isolated rat heart atria, although to a much lesser extent than 6-hydroxydopamine.
    DOI:
    10.1021/jm00197a008
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文献信息

  • A Convenient Access to Dihydroxybenzenethiols<i>via</i>Reduction of<i>Iso</i>-Thiouronium Salts with Sodium Borohydride
    作者:D. Mascagna、M. d'Ischia、C. Costantini、G. Prota
    DOI:10.1080/00397919408012622
    日期:1994.1
    Abstract An improved procedure for the preparation of unstable dihydroxybenzenethiols in high yields is reported, involving mild reduction of the corresponding iso-thiouronium salts with sodium borohydride.
    摘要 报道了一种以高产率制备不稳定二羟基苯硫醇的改进方法,包括用硼氢化钠温和还原相应的异硫脲盐。
  • Mascagna D., dIschia M., Costantini C., Prota G., Synth. Commun, 24 (1994) N 1, S 35- 42
    作者:Mascagna D., dIschia M., Costantini C., Prota G.
    DOI:——
    日期:——
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