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Methanesulfonic acid 2-ethoxy-4-formyl-phenyl ester

中文名称
——
中文别名
——
英文名称
Methanesulfonic acid 2-ethoxy-4-formyl-phenyl ester
英文别名
(2-ethoxy-4-formylphenyl) methanesulfonate
Methanesulfonic acid 2-ethoxy-4-formyl-phenyl ester化学式
CAS
——
化学式
C10H12O5S
mdl
MFCD13874057
分子量
244.268
InChiKey
HTYSZVHRFXGDIN-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):
    1.3
  • 重原子数:
    16
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    78
  • 氢给体数:
    0
  • 氢受体数:
    5

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

  • 作为产物:
    描述:
    乙基香兰素甲基磺酰氯4-二甲氨基吡啶 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以100%的产率得到Methanesulfonic acid 2-ethoxy-4-formyl-phenyl ester
    参考文献:
    名称:
    Benzothiazole, thiazolopyridine, benzooxazole and oxazolopyridine derivatives
    摘要:
    这项发明涉及以下式的化合物 其中A、B 1 、B 2 、R 1 、R 2 和G如描述和索赔中所定义,并其药学上可接受的盐。该发明还涉及含有这种化合物的药物组合物,以及用于制备它们的方法和它们用于治疗和/或预防与调节SST受体亚型5相关的疾病的用途。
    公开号:
    US20060205718A1
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文献信息

  • Pyrimidine, quinazoline, pteridine and triazine derivatives
    申请人:Binggeli Alfred
    公开号:US20070225271A1
    公开(公告)日:2007-09-27
    This invention is concerned with compounds of the formula wherein A, R 1 to R 5 and G are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The invention further relates to pharmaceutical compositions containing such compounds, to a process for their preparation and to their use for the treatment and/or prevention of diseases which are associated with the modulation of SST receptors subtype 5.
    这项发明涉及以下式的化合物 其中A,R1至R5和G如描述和声明中所定义,并其药学上可接受的盐。该发明还涉及含有这种化合物的药物组合物,以及用于制备它们的方法和它们用于治疗和/或预防与调节SST受体亚型5相关的疾病的用途。
  • Benzothiazole, thiazolopyridine, benzooxazole and oxazolopyridine derivatives
    申请人:Binggeli Alfred
    公开号:US20060205718A1
    公开(公告)日:2006-09-14
    This invention is concerned with compounds of the formula wherein A, B 1 , B 2 , R 1 , R 2 and G are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The invention further relates to pharmaceutical compositions containing such compounds, to a process for their preparation and to their use for the treatment and/or prevention of diseases which are associated with the modulation of SST receptors subtype 5.
    这项发明涉及以下式的化合物 其中A、B 1 、B 2 、R 1 、R 2 和G如描述和索赔中所定义,并其药学上可接受的盐。该发明还涉及含有这种化合物的药物组合物,以及用于制备它们的方法和它们用于治疗和/或预防与调节SST受体亚型5相关的疾病的用途。
  • Pyrimidine and quinazoline derivatives
    申请人:Christ Andreas D.
    公开号:US20080045550A1
    公开(公告)日:2008-02-21
    This invention is concerned with compounds of the formula wherein A, R 1 to R 5 and G are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The invention further relates to pharmaceutical compositions containing such compounds, to a process for their preparation and to their use for the treatment and/or prevention of diseases which are associated with the modulation of SST receptors subtype 5.
    本发明涉及以下式子的化合物,其中A,R1到R5和G的定义如描述和权利要求中所述,并且其药学上可接受的盐。本发明还涉及含有这些化合物的制药组合物,以及其制备过程和用于治疗和/或预防与SST受体亚型5调节相关的疾病的用途。
  • Pyrimidine and Quinazoline Derivatives
    申请人:Christ Andreas D.
    公开号:US20100069413A1
    公开(公告)日:2010-03-18
    This invention is concerned with compounds of the formula wherein A, R 1 to R 5 and G are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The invention further relates to pharmaceutical compositions containing such compounds, to a process for their preparation and to their use for the treatment and/or prevention of diseases which are associated with the modulation of SST receptors subtype 5.
    本发明涉及公式中的化合物,其中A、R1至R5和G如描述和权利要求中所定义,并且其药学上可接受的盐。本发明还涉及含有这些化合物的药物组合物,以及制备它们的过程和它们用于治疗和/或预防与SST受体亚型5调节相关的疾病的用途。
  • Substituted piperidine derivatives as SST5 modulators
    申请人:Hoffmann-La Roche Inc.
    公开号:US07968568B2
    公开(公告)日:2011-06-28
    This invention is concerned with compounds of the formula wherein A, R1 to R5 and G are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The invention further relates to pharmaceutical compositions containing such compounds, to a process for their preparation and to their use for the treatment and/or prevention of diseases which are associated with the modulation of SST receptors subtype 5.
    本发明涉及以下式子的化合物,其中A,R1到R5和G的定义如说明书和权利要求所述,并且其药学上可接受的盐。本发明还涉及包含这些化合物的药物组合物,以及制备它们的过程和它们用于治疗和/或预防与SST受体亚型5调节相关的疾病的用途。
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