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3-(3-methoxythiophen-2-yl)propionic acid | 1528736-53-9

中文名称
——
中文别名
——
英文名称
3-(3-methoxythiophen-2-yl)propionic acid
英文别名
3-(3-Methoxythiophen-2-yl)propanoic acid
3-(3-methoxythiophen-2-yl)propionic acid化学式
CAS
1528736-53-9
化学式
C8H10O3S
mdl
——
分子量
186.232
InChiKey
YYIYBZQQBRWJRR-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):
    1.4
  • 重原子数:
    12
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    74.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    4-(bis[tert-butoxycarbonyl]amino)-6-amino-2-methylquinoline 、 3-(3-methoxythiophen-2-yl)propionic acidN,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 16.0h, 生成 N-(4-amino-2-methylquinolin-6-yl)-3-(3-methoxythiophene-2-yl)propionamide trifluoroacetate
    参考文献:
    名称:
    Small molecule inhibitors of anthrax lethal factor toxin
    摘要:
    This manuscript describes the preparation of new small molecule inhibitors of Bacillus anthracis lethal factor. Our starting point was the symmetrical, bis-quinolinyl compound 1 (NSC 12155). Optimization of one half of this molecule led to new LF inhibitors that were desymmetrized to afford more drug-like compounds. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.11.009
  • 作为产物:
    描述:
    3-甲氧基噻吩-2-甲醛 在 5% rhodium on activated aluminium oxide 、 potassium tert-butylate氢气 、 potassium hydroxide 作用下, 以 四氢呋喃甲醇乙酸乙酯 为溶剂, -78.0~60.0 ℃ 、262.01 kPa 条件下, 反应 168.75h, 生成 3-(3-methoxythiophen-2-yl)propionic acid
    参考文献:
    名称:
    Small molecule inhibitors of anthrax lethal factor toxin
    摘要:
    This manuscript describes the preparation of new small molecule inhibitors of Bacillus anthracis lethal factor. Our starting point was the symmetrical, bis-quinolinyl compound 1 (NSC 12155). Optimization of one half of this molecule led to new LF inhibitors that were desymmetrized to afford more drug-like compounds. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.11.009
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文献信息

  • US4571437A
    申请人:——
    公开号:US4571437A
    公开(公告)日:1986-02-18
  • Small molecule inhibitors of anthrax lethal factor toxin
    作者:John D. Williams、Atiyya R. Khan、Steven C. Cardinale、Michelle M. Butler、Terry L. Bowlin、Norton P. Peet
    DOI:10.1016/j.bmc.2013.11.009
    日期:2014.1
    This manuscript describes the preparation of new small molecule inhibitors of Bacillus anthracis lethal factor. Our starting point was the symmetrical, bis-quinolinyl compound 1 (NSC 12155). Optimization of one half of this molecule led to new LF inhibitors that were desymmetrized to afford more drug-like compounds. (C) 2013 Elsevier Ltd. All rights reserved.
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