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7-(2-Ethyl-1-Hexen-1-yl)-8-quinolinol

中文名称
——
中文别名
——
英文名称
7-(2-Ethyl-1-Hexen-1-yl)-8-quinolinol
英文别名
7-[(E)-2-ethylhex-1-enyl]quinolin-8-ol
7-(2-Ethyl-1-Hexen-1-yl)-8-quinolinol化学式
CAS
——
化学式
C17H21NO
mdl
——
分子量
255.36
InChiKey
KVXNGMXXHWBFRX-OUKQBFOZSA-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):
    5.4
  • 重原子数:
    19
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    33.1
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    参考文献:
    名称:
    Substituted 8-hydroxyquinolines and process for the preparation thereof
    摘要:
    一类羟基喹啉的烃基取代物,其中所示取代基是通过采用障碍醛对该喹啉酚进行间接烷基化而产生的。这些烷基化物在水冶提取过程中是有用的金属收集剂,旨在从稀释的水溶液中回收金属价值。
    公开号:
    US04066652A1
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文献信息

  • Substituted 8-hydroxyquinolines and process for the preparation thereof
    申请人:Ashland Oil, Inc.
    公开号:US04066652A1
    公开(公告)日:1978-01-03
    A class of hydrocarbyl substituted 8-hydroxyquinolines wherein the indicated substituent arises through the indirect alkylation of said quinolinol with a hindered aldehyde. These alkylates are useful metal collectors in hydrometallurgical extraction processes designed for the recovery of metal values from dilute aqueous solutions thereof.
    一类羟基喹啉的烃基取代物,其中所示取代基是通过采用障碍醛对该喹啉酚进行间接烷基化而产生的。这些烷基化物在水冶提取过程中是有用的金属收集剂,旨在从稀释的水溶液中回收金属价值。
  • [EN] METHOD FOR TREATING DRUG-RESISTANT BACTERIAL AND OTHER INFECTIONS WITH CLIOQUINOL, PHANQUINONE, AND RELATED COMPOUNDS<br/>[FR] PROCÉDÉ POUR TRAITER DES INFECTIONS BACTÉRIENNES RÉSISTANT AU MÉDICAMENT ET D'AUTRES INFECTIONS PAR DU CLIOQUINOL, DE LA PHANQUINONE ET DES COMPOSÉS APPARENTÉS
    申请人:XILINAS MICHEL E
    公开号:WO2009140215A2
    公开(公告)日:2009-11-19
    The invention relates to new uses of known chelating compounds for the treatment of bacterial in fungal infections, particularly by methicilllin-resistant and other drug-resistant strains of bacteria and fungi. One of more chelating compound is administered with or without additional antibiotic or antifungal drugs to achieve improved therapy. Preferred chelating compounds include clioquinol, 5,7-dichloro-8-hydroxy-quinaldine, phanquinone, 5,7-dichloro-8-hydroxyquinoline, 5,7- di-iodo-8-hydroxyquinoline. By chelation of specific metal ions, these compounds treat any infection by bacteria or fungi whose pathogenicity depends upon metalloenzymes that require these cations. The compounds are also effective against infections caused by extended β lactamase and metallo β lactamase producing bacterial strains. Bacteria targeted by these methods include methicillin-resistant Staphylococcus aureus, penicillin resistant or intermediate resistant Streptococcus pneumoniae and other gram positive and multiresistant gram negative species and strains.
  • LIU, CHANG-JI;SHU, GUO-EN;YUAN, CHENG-YE, ACTA CHIM. SIN, 1983, 41, N 7, 654-658
    作者:LIU, CHANG-JI、SHU, GUO-EN、YUAN, CHENG-YE
    DOI:——
    日期:——
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