摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-[2-(3-Methoxyphenyl)ethoxy]acetic acid | 1267967-52-1

中文名称
——
中文别名
——
英文名称
2-[2-(3-Methoxyphenyl)ethoxy]acetic acid
英文别名
2-[2-(3-methoxyphenyl)ethoxy]acetic acid
2-[2-(3-Methoxyphenyl)ethoxy]acetic acid化学式
CAS
1267967-52-1
化学式
C11H14O4
mdl
——
分子量
210.23
InChiKey
YTKLUNNXFIJQHJ-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):
    1.6
  • 重原子数:
    15
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    55.8
  • 氢给体数:
    1
  • 氢受体数:
    4

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

  • 作为反应物:
    描述:
    2-[2-(3-Methoxyphenyl)ethoxy]acetic acid草酰氯N,N-二甲基甲酰胺 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 生成
    参考文献:
    名称:
    Pyrido pyrimidinones as selective agonists of the high affinity niacin receptor GPR109A: Optimization of in vitro activity
    摘要:
    Pyrido pyrimidinones are selective agonists of the human high affinity niacin receptor GPR109A (HM74A). They show no activity on the highly homologous low affinity receptor GPR109B (HM74). Starting from a high throughput screening hit the in vitro activity of the pyrido pyrimidinones was significantly improved providing lead compounds suitable for further optimization. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.07.108
  • 作为产物:
    描述:
    2-(3-甲氧基苯基)乙醇氯乙酸 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 生成 2-[2-(3-Methoxyphenyl)ethoxy]acetic acid
    参考文献:
    名称:
    Pyrido pyrimidinones as selective agonists of the high affinity niacin receptor GPR109A: Optimization of in vitro activity
    摘要:
    Pyrido pyrimidinones are selective agonists of the human high affinity niacin receptor GPR109A (HM74A). They show no activity on the highly homologous low affinity receptor GPR109B (HM74). Starting from a high throughput screening hit the in vitro activity of the pyrido pyrimidinones was significantly improved providing lead compounds suitable for further optimization. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.07.108
点击查看最新优质反应信息

文献信息

  • Pyrido pyrimidinones as selective agonists of the high affinity niacin receptor GPR109A: Optimization of in vitro activity
    作者:Jens-Uwe Peters、Holger Kühne、Henrietta Dehmlow、Uwe Grether、Aurelia Conte、Dominik Hainzl、Cornelia Hertel、Nicole A. Kratochwil、Michael Otteneder、Robert Narquizian、Constantinos G. Panousis、Fabienne Ricklin、Stephan Röver
    DOI:10.1016/j.bmcl.2010.07.108
    日期:2010.9
    Pyrido pyrimidinones are selective agonists of the human high affinity niacin receptor GPR109A (HM74A). They show no activity on the highly homologous low affinity receptor GPR109B (HM74). Starting from a high throughput screening hit the in vitro activity of the pyrido pyrimidinones was significantly improved providing lead compounds suitable for further optimization. (c) 2010 Elsevier Ltd. All rights reserved.
查看更多