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1-(4-(萘-1-氧基)苯基)乙酮 | 93291-63-5

中文名称
1-(4-(萘-1-氧基)苯基)乙酮
中文别名
——
英文名称
1-(4-(naphthalen-1-yloxy)phenyl)ethanone
英文别名
1-(4-(naphthalen-1-yloxy)phenyl)ethan-1-one;1-(4-Naphthalen-1-yloxyphenyl)ethanone
1-(4-(萘-1-氧基)苯基)乙酮化学式
CAS
93291-63-5
化学式
C18H14O2
mdl
——
分子量
262.308
InChiKey
MMMVHEKKGHIVIV-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

物化性质

  • 沸点:
    430.1±28.0 °C(Predicted)
  • 密度:
    1.162±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1-(4-(萘-1-氧基)苯基)乙酮 生成 2,2-Dihydroxy-1-(4-naphthalen-1-yloxyphenyl)ethanone
    参考文献:
    名称:
    FLOYD, M. B,, JR.;DEVRIES, V. G.
    摘要:
    DOI:
  • 作为产物:
    描述:
    4-氟苯乙酮甲醇 、 sodium tetrahydroborate 、 RuH2(CO)(PPh3)3potassium carbonate1,2-双(二苯基膦)乙烷 作用下, 以 二甲基亚砜丙酮 为溶剂, 反应 48.0h, 生成 1-(4-(萘-1-氧基)苯基)乙酮
    参考文献:
    名称:
    探索串联钌催化的氢转移和S N Ar化学
    摘要:
    报道了一种通过电子芳烃活化对苯甲醇进行催化官能化的氢转移策略,该方法以优异的分离产率获得了各种定制的二芳基醚和芳基胺(38例,平均产率为70%)。利用氢转移方法,可以通过明智地选择简单和廉价的添加剂来选择功能化产物的氧化水平。
    DOI:
    10.1021/acs.orglett.7b03441
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文献信息

  • Substituted arylglyoxal derivatives
    申请人:AMERICAN CYANAMID COMPANY
    公开号:EP0114389A2
    公开(公告)日:1984-08-01
    Arylglyoxals which are new compounds and which are active as hypoglycemic agents.
    芳基乙二醛是一种新化合物,具有降血糖剂的活性。
  • SAR-Based Optimization of a 4-Quinoline Carboxylic Acid Analogue with Potent Antiviral Activity
    作者:Priyabrata Das、Xiaoyi Deng、Liang Zhang、Michael G. Roth、Beatriz M. A. Fontoura、Margaret A. Phillips、Jef K. De Brabander
    DOI:10.1021/ml300464h
    日期:2013.6.13
    It is established that drugs targeting viral proteins are at risk of generating resistant strains. However, drugs targeting host factors can potentially avoid this problem. Herein, we report structure-ctivity relationship studies leading to the discovery of a very potent lead compound 6-fluoro-2-(5-isopropyl-2-methyl-4-phenoxyphenyl) quinoline -4-carboxylic acid (C44) that inhibits human dihydroorotate dehydrogenase (DHODH) with an IC50 of 1 nM and viral replication of VSV and WSN-Influenza with an EC50 of 2 nM and 41 nM. We also solved the X-ray structure of human DHODH bound to C44, providing structural insight into the potent inhibition of biaryl ether analogues of brequinar.
  • 6-(4′-Aryloxy-phenyl)vinyl-1,2,4-trioxanes: A new series of orally active peroxides effective against multidrug-resistant Plasmodium yoelii in Swiss mice
    作者:Chandan Singh、Ved Prakash Verma、Niraj Krishna Naikade、Ajit Shankar Singh、Mohammad Hassam、Sunil. K. Puri
    DOI:10.1016/j.bmcl.2010.06.045
    日期:2010.8
    A new series of 6-(4'-aryloxy-phenyl)vinyl-1,2,4-trioxanes 10a-d, 11a-d, and 12a-d have been synthesized and evaluated for their antimalarial activity against multidrug-resistant Plasmodium yoelii in Swiss mice by oral route. Trioxanes 10b and 10c, the two most active compounds of the series, provided 100% protection to the infected mice at 48 mg/kg x 4 days. Clinically useful drug beta-arteether provided 100% and 20% protection at 48 mg/kg x 4 days and 24 mg/kg x 4 days, respectively, in this model. (C) 2010 Elsevier Ltd. All rights reserved.
  • FLOYD, M. B,, JR.;DEVRIES, V. G.
    作者:FLOYD, M. B,, JR.、DEVRIES, V. G.
    DOI:——
    日期:——
  • US4474810A
    申请人:——
    公开号:US4474810A
    公开(公告)日:1984-10-02
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