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1-(2,4-Difluoro-5-methylphenyl)ethanone | 177211-27-7

中文名称
——
中文别名
——
英文名称
1-(2,4-Difluoro-5-methylphenyl)ethanone
英文别名
——
1-(2,4-Difluoro-5-methylphenyl)ethanone化学式
CAS
177211-27-7
化学式
C9H8F2O
mdl
——
分子量
170.16
InChiKey
LUWOUTWVUKRWGY-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:
    218.7±35.0 °C(Predicted)
  • 密度:
    1.168±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • 2-Alkynyl-and 2-alkenyl-pyrazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pyrimidine adenosine A2a receptor antagonists
    申请人:Schering Corporation
    公开号:US20040220194A1
    公开(公告)日:2004-11-04
    Compounds having the structural formula I 1 or a pharmaceutically acceptable salt thereof, wherein R is 2 R 1 , R 2 , R 3 , R 4 and R 5 are H, alkyl or alkoxyalkyl; R 6 is H, alkyl, hydroxyalkyl or —CH 2 F; R 7 , R 8 and R 9 are H, alkyl, alkoxy, alkylthio, alkoxyalkyl, halo or —CF 3 ; and Z is optionally substituted aryl, heteroaryl or heteroaryl-alkyl are disclosed. Also disclosed is the use of compounds of formula I in the treatment of central nervous system diseases, in particular Parkinson's disease, alone or in combination with other agents for treating Parkinson's disease, and pharmaceutical compositions comprising them.
    具有结构式I或其药用可接受盐的化合物,其中R是R1,R2,R3,R4和R5为H,烷基或烷氧基烷基;R6为H,烷基,羟基烷基或—CH2F;R7,R8和R9为H,烷基,烷氧基,烷硫基,烷氧基烷基,卤素或—CF3;以及Z是可选择地取代的芳基,杂环芳基或杂环芳基烷基。还公开了化合物I的应用于治疗中枢神经系统疾病,特别是帕金森病,单独或与其他治疗帕金森病的药剂联合使用,以及包含它们的药物组合物。
  • 2-ALKYNYL-AND 2-ALKENYL-PYRAZOLO- [4,3-E ] -1,2,4-TRIAZOLO- [1,5-C] -PYRIMIDINE ADENOSINE A2A RECEPTOR ANTAGONISTS
    申请人:Schering Corporation
    公开号:EP1622912B1
    公开(公告)日:2009-05-27
  • US7709492B2
    申请人:——
    公开号:US7709492B2
    公开(公告)日:2010-05-04
  • [EN] PYRAZOLO-[4,3-e]-1,2,4-TRIAZOLO-[1,5-c]-PYRIMIDINE ADENOSINE A2A RECEPTOR ANTAGONISTS<br/>[FR] ANTAGONISTES DU RECEPTEUR A2A DE L'ADENOSINE A BASE DE PYRAZOLO-[4,3-E]-1,2,4-TRIAZOLO-[1,5-C]-PYRIMIDINE
    申请人:SCHERING CORP
    公开号:WO2005103055A1
    公开(公告)日:2005-11-03
    Compounds having the structural formula I or a pharmaceutically acceptable salt thereof, wherein R is optionally substituted phenyl, furanyl, thienyl, pyridyl, pyridyl N-oxide, oxazolyl or pyrrolyl, or cycloalkenyl R1, R2, R3, R4 and R5 are H, alkyl or alkoxyalkyl; and Z is optionally substituted aryl or heteroaryl are disclosed. Also disclosed is the use of compounds of formula I in the treatment of central nervous system diseases, in particular Parkinson's disease, alone or in combination with other agents for treating Parkinson's disease, and pharmaceutical compositions comprising them.
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