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8-(3-methoxybenzyloxy)quinoline

中文名称
——
中文别名
——
英文名称
8-(3-methoxybenzyloxy)quinoline
英文别名
8-[(3-Methoxyphenyl)methoxy]quinoline
8-(3-methoxybenzyloxy)quinoline化学式
CAS
——
化学式
C17H15NO2
mdl
——
分子量
265.312
InChiKey
LUTQZGMUQYKORM-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):
    3.5
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    31.4
  • 氢给体数:
    0
  • 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

反应信息

  • 作为产物:
    描述:
    8-羟基喹啉 、 alkaline earth salt of/the/ methylsulfuric acid 在 四丁基溴化铵 、 potassium hydroxide 作用下, 以 二氯甲烷 为溶剂, 以36%的产率得到8-(3-methoxybenzyloxy)quinoline
    参考文献:
    名称:
    Development of 8-benzyloxy-substituted quinoline ethers and evaluation of their antimicrobial activities
    摘要:
    A series of 8-benzyloxy-substituted quinoline ethers (2a-n) compounds were synthesized. All synthesized compounds were screened in vitro for their preliminary antimicrobial activities against two Gram-negative bacteria (Pseudomonas aeruginosa and Escherichia coli), two Gram-positive bacteria (Staphylococcus aureus and Staphylococcus epidermidis), and a fungal species (Aspergillus niger). Among all synthesized compounds, compound 2e showed a significant growth inhibitory activity with MIC value 3.125 mu g/mL which was comparable to 8-hydroxyquinoline (2.5 mu g/mL) and terbinafine (1.25 mu g/mL) against A. niger.
    DOI:
    10.1007/s00044-014-1217-4
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文献信息

  • [EN] NOVEL 6-PHENYLPHENANTHRIDINES<br/>[FR] NOUVELLES 6-PHENYLPHENANTHRIDINES
    申请人:ALTANA PHARMA AG
    公开号:WO2005012253A1
    公开(公告)日:2005-02-10
    Compounds of a certain formula (I), in which R1, R2, R3, R31, R4, R5, R51, R6, R7 and R8 have the meanings indicated in the description, are novel effective PDE4 inhibitors.
    具有以下含义的化合物(I),其中R1、R2、R3、R31、R4、R5、R51、R6、R7和R8的含义如说明书所示,是新型有效的PDE4抑制剂。
  • NOVEL 6-PHENYLPHENANTHRIDINES
    申请人:ALTANA Pharma AG
    公开号:EP1658271A1
    公开(公告)日:2006-05-24
  • Development of 8-benzyloxy-substituted quinoline ethers and evaluation of their antimicrobial activities
    作者:Po-Yee Chung、Roberto Gambari、Yi-Xin Chen、Chor-Hing Cheng、Zhao-Xiang Bian、Albert Sun-Chi Chan、Johnny Cheuk-On Tang、Polly Hang-Mei Leung、Chung-Hin Chui、Kim-Hung Lam
    DOI:10.1007/s00044-014-1217-4
    日期:2015.4
    A series of 8-benzyloxy-substituted quinoline ethers (2a-n) compounds were synthesized. All synthesized compounds were screened in vitro for their preliminary antimicrobial activities against two Gram-negative bacteria (Pseudomonas aeruginosa and Escherichia coli), two Gram-positive bacteria (Staphylococcus aureus and Staphylococcus epidermidis), and a fungal species (Aspergillus niger). Among all synthesized compounds, compound 2e showed a significant growth inhibitory activity with MIC value 3.125 mu g/mL which was comparable to 8-hydroxyquinoline (2.5 mu g/mL) and terbinafine (1.25 mu g/mL) against A. niger.
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