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1-chloro-3-(propylsulfanyl)propan-2-ol

中文名称
——
中文别名
——
英文名称
1-chloro-3-(propylsulfanyl)propan-2-ol
英文别名
1-chloro-3-propanylthiopropan-2-ol;n-Propyl-(3-chlor-2-hydroxypropyl)-sulfid;1-Chlor-3-propylmercapto-propan-2-ol;Propyl-(3-chlor-2-hydroxy-propyl)-sulfid;1-Chloro-3(propylsulfanyl)propan-2-ol;1-chloro-3-propylsulfanylpropan-2-ol
1-chloro-3-(propylsulfanyl)propan-2-ol化学式
CAS
——
化学式
C6H13ClOS
mdl
——
分子量
168.688
InChiKey
ZBJZFKVFPDUIIH-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:
    9
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    45.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1-chloro-3-(propylsulfanyl)propan-2-ol 在 sodium hydroxide 作用下, 以 为溶剂, 生成 1-(p-tolyloxy)-3-(propylsulfanyl)-2-(N,N-diethylaminomethoxy)propane
    参考文献:
    名称:
    Synthesis and Properties of Aminomethoxy Derivatives of 1-(p-Tolyloxy)-3-(propylsulfanyl)propane
    摘要:
    Mannich condensation of 1-(p-tolyloxy)-3-(propylsulfanyl)propane-2-ol with formaldehyde and secondary amines leads to the formation of new aminomethoxy derivatives of 1-(p-tolyloxy)-3-(propylsulfanyl)propane in yield of 68-80%. Antimicrobial activity of the obtained compounds was investigated.
    DOI:
    10.1134/s1070363220010090
  • 作为产物:
    参考文献:
    名称:
    Nenitzescu; Scarlatescu, Chemische Berichte, 1935, vol. 68, p. 587,590
    摘要:
    DOI:
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文献信息

  • Nenitzescu; Scarlatescu, Chemische Berichte, 1935, vol. 68, p. 587,590
    作者:Nenitzescu、Scarlatescu
    DOI:——
    日期:——
  • Synthesis and Properties of Aminomethoxy Derivatives of 1-Phenoxy-3-(propylsulfanyl)propane
    作者:I. A. Jafarov、E. H. Mammadbayli、K. A. Kochetkov、A. D. Astanova、L. M. Maharramova
    DOI:10.1134/s1070428019090021
    日期:2019.9
    The condensation of 1-phenoxy-3-(propylsulfanyl)propan-2-ol with formaldehyde and secondary aliphatic and heterocyclic amines afforded new aminomethoxy derivatives of 1-phenoxy-3-(propylsulfanyl)- propane in 69-77% yields. The product structure was confirmed by elemental analyses and IR and H-1 and C-13 NMR spectra. The synthesized compounds were assayed as antiseptics against bacteria and fungi and were shown to be more efficient antimicrobial agents than those currently used in medicine.
  • Some β-Hydroxypropyl Sulfides and their Derivatives<sup>1</sup>
    作者:Thomas K. Todsen、C. B. Pollard、Edward G. Rietz
    DOI:10.1021/ja01165a046
    日期:1950.9
  • Synthesis and Properties of Aminomethoxy Derivatives of 1-(p-Tolyloxy)-3-(propylsulfanyl)propane
    作者:E. H. Mammadbayli、I. A. Jafarov、A. D. Astanova、L. M. Maharramova、N. A. Jafarova
    DOI:10.1134/s1070363220010090
    日期:2020.1
    Mannich condensation of 1-(p-tolyloxy)-3-(propylsulfanyl)propane-2-ol with formaldehyde and secondary amines leads to the formation of new aminomethoxy derivatives of 1-(p-tolyloxy)-3-(propylsulfanyl)propane in yield of 68-80%. Antimicrobial activity of the obtained compounds was investigated.
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