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3-Chloro-4-ethoxybenzeneacetyl chloride | 373361-72-9

中文名称
——
中文别名
——
英文名称
3-Chloro-4-ethoxybenzeneacetyl chloride
英文别名
2-(3-chloro-4-ethoxyphenyl)acetyl chloride
3-Chloro-4-ethoxybenzeneacetyl chloride化学式
CAS
373361-72-9
化学式
C10H10Cl2O2
mdl
——
分子量
233.09
InChiKey
YGIBGLUYNJLKJL-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):
    2.9
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • INDAZOLES SUBSTITUTED WITH1,1-DIOXOISOTHIAZOLIDINE USEFUL AS INHIBITORS OF CELL PROLIFERATION
    申请人:——
    公开号:US20030149034A1
    公开(公告)日:2003-08-07
    The present invention relates to an indazole derivative, pharmaceutically acceptable salt, solvated product and isomer thereof substituted with 1,1-dioxoisothiazolidine which are useful as inhibitors for Cyclin Dependent Kinase (CDK). The present invention also relates to an agent for inhibiting and treating diseases involving cell proliferation, e.g., cancer, inflammation, restenosis, angiogenesis, etc. which comprises the compound of formula (1) as an active ingredient together with a pharmaceutically acceptable carrier.
    本发明涉及一种与1,1-二氧异噻唑啉基取代的吲唑啉衍生物、药用可接受的盐、溶剂化产物和同分异构体,其作为 Cyclin Dependent Kinase (CDK) 的抑制剂。本发明还涉及一种用于抑制和治疗涉及细胞增殖的疾病,例如癌症、炎症、再狭窄、血管生成等的药剂,其包括化合物(1)的配方作为活性成分,与药用可接受的载体一起使用。
  • EP1280802A4
    申请人:——
    公开号:EP1280802A4
    公开(公告)日:2003-06-11
  • INDAZOLES SUBSTITUTED WITH 1,1-DIOXOISOTHIAZOLIDINE USEFUL AS INHIBITORS OF CELL PROLIFERATION
    申请人:LG Life Sciences Ltd.
    公开号:EP1280802A1
    公开(公告)日:2003-02-05
  • US6620831B2
    申请人:——
    公开号:US6620831B2
    公开(公告)日:2003-09-16
  • [EN] INDAZOLES SUBSTITUTED WITH 1,1-DIOXOISOTHIAZOLIDINE USEFUL AS INHIBITORS OF CELL PROLIFERATION<br/>[FR] INDAZOLES SUBSTITUES AVEC DE LA 1,1-DIOXOISOTHIAZOLIDINE UTILES COMME INHIBITEURS DE LA PROLIFERATION CELLULAIRE
    申请人:LG CHEM INVESTMENT LTD
    公开号:WO2001085726A1
    公开(公告)日:2001-11-15
    The present invention relates to an indazole derivative, pharmaceutically acceptable salt, solvated product and isomer thereof substituted with 1,1-dioxoisothiazolidine which are useful as inhibitors for Cyclin Dependent Kinase(CDK). The present invention also relates to an agent for inhibiting and treating diseases involving cell proliferation, e.g., cancer, inflammation, restenosis, angiogenesis, etc. which comprises the indazole derivative as an active ingredient together with a pharmaceutically acceptable carrier.
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