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2-Chlor-5-hydroxy-4-methoxy-benzaldehyd | 89938-55-6

中文名称
——
中文别名
——
英文名称
2-Chlor-5-hydroxy-4-methoxy-benzaldehyd
英文别名
2-chloro-4-methoxy-5-hydroxybenzaldehyde;2-Chloro-5-hydroxy-4-methoxybenzaldehyde
2-Chlor-5-hydroxy-4-methoxy-benzaldehyd化学式
CAS
89938-55-6
化学式
C8H7ClO3
mdl
——
分子量
186.595
InChiKey
GCWUQIASOQMXGR-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):
    2.1
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Organic Compounds
    申请人:Ehrhardt Claus
    公开号:US20080194549A1
    公开(公告)日:2008-08-14
    The invention relates to the use of (3,4-di-, 3,3,4-tri, 3,4,4-tri- or 3,3,4,4-tetra-)substituted pyrrolidine compounds for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; compounds that are part of a subclass of these substituted pyrrolidine compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (=disorder) that depends on activity of renin; new compounds that are part of a subclass of these substituted pyrrolidine compounds; pharmaceutical formulations comprising said substituted pyrrolidine compounds, and/or a method of treatment comprising administering said substituted pyrrolidine compounds, a method for the manufacture especially of said new substituted pyrrolidine compounds, as well as novel intermediates, starting materials and/or partial steps for their synthesis.
    本发明涉及使用(3,4-二-, 3,3,4-三-, 3,4,4-三-或3,3,4,4-四-)取代吡咯烷化合物制备治疗依赖于肾素活性的疾病的药物制剂;使用该类化合物治疗依赖于肾素活性的疾病;该取代吡咯烷化合物亚类的化合物用于温血动物的诊断和治疗,特别是用于治疗依赖于肾素活性的疾病;该取代吡咯烷化合物亚类的新化合物;包括所述取代吡咯烷化合物的药物制剂和/或包括给予所述取代吡咯烷化合物的治疗方法,特别是制备该新取代吡咯烷化合物的方法,以及其合成的新中间体、起始材料和/或部分步骤。
  • PYRAZOLO-HETEROARYL COMPOUNDS
    申请人:Revesz Lászlo
    公开号:US20090258874A1
    公开(公告)日:2009-10-15
    A compound of formula I wherein the groups R1-R4, X and Y are as defined in the specification, useful to treat TNF-Alpha and IL-1 mediated diseases.
    化合物I的公式为其中R1-R4,X和Y的基团如规范中所定义,可用于治疗TNF-Alpha和IL-1介导的疾病。
  • AMIDE DERIVATIVE
    申请人:Nakahira Hiroyuki
    公开号:US20100056497A1
    公开(公告)日:2010-03-04
    The present invention relates to a compound of the formula (I) being useful as a renin inhibitor, or a pharmaceutically acceptable salt thereof. wherein R 1a is a hydrogen atom, an optionally substituted C 1-6 alkyl, etc.; R 1b is an optionally substituted C 1-6 alkoxy, etc.; R 1c is a hydrogen atom, an optionally substituted C 1-6 alkoxy, etc.; R 2 is a hydrogen atom, an optionally substituted C 1-6 alkyl, etc.; R 3a , R 3b , R 3c and R 3d are independently the same or different, and each is a group of the formula: -A-B (in which A is a single bond, —(CH 2 ) s O—, —(CH 2 ) s N(R 4 )CO—, etc., B is a hydrogen atom, an optionally substituted C 1-6 alkyl, etc.), etc.; R 4 is a hydrogen atom, an optionally substituted C 1-6 alkyl, etc.; s is 0, etc.; and n is 1, etc.
    本发明涉及一种具有式(I)的化合物,其可用作肾素抑制剂,或其药学上可接受的盐。其中,R1a是氢原子,可选地取代的C1-6烷基等;R1b是可选地取代的C1-6烷氧基等;R1c是氢原子,可选地取代的C1-6烷氧基等;R2是氢原子,可选地取代的C1-6烷基等;R3a,R3b,R3c和R3d独立且相同或不同,每个是式:-A-B的基团(其中A是单键,-(CH2)sO-,-(CH2)sN(R4)CO-等,B是氢原子,可选地取代的C1-6烷基等)等;R4是氢原子,可选地取代的C1-6烷基等;s为0等;n为1等。
  • Organic compounds
    申请人:Novartis AG
    公开号:US07807709B2
    公开(公告)日:2010-10-05
    The invention relates to the use of (3,4-di-, 3,3,4-tri, 3,4,4-tri- or 3,3,4,4-tetra-)substituted pyrrolidine compounds for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; compounds that are part of a subclass of these substituted pyrrolidine compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (=disorder) that depends on activity of renin; new compounds that are part of a subclass of these substituted pyrrolidine compounds; pharmaceutical formulations comprising said substituted pyrrolidine compounds, and/or a method of treatment comprising administering said substituted pyrrolidine compounds, a method for the manufacture especially of said new substituted pyrrolidine compounds, as well as novel intermediates, starting materials and/or partial steps for their synthesis.
    本发明涉及使用(3,4-二-, 3,3,4-三-, 3,4,4-三-或3,3,4,4-四-)取代吡咯烷化合物来制备用于治疗依赖于肾素活性的疾病的药物制剂;该类化合物在治疗依赖于肾素活性的疾病中的使用;属于这些取代吡咯烷化合物亚类的化合物用于诊断和治疗温血动物,特别是用于治疗依赖于肾素活性的疾病(=失调);属于这些取代吡咯烷化合物亚类的新化合物;包含所述取代吡咯烷化合物的药物制剂,和/或包括给予所述取代吡咯烷化合物的治疗方法,一种用于特别制备这些新的取代吡咯烷化合物的方法,以及其合成的新中间体,起始材料和/或部分步骤。
  • PYRAZOLO-HETEROARYL COMPOUNDS USEFUL TO TREAT TNF-ALPHA AND IL-1 MEDIATED DISEASES
    申请人:Novartis AG
    公开号:EP1833477B1
    公开(公告)日:2010-06-02
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