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ethyl 2-(3-fluoro-4-hydroxyphenyl)acetate | 259543-80-1

中文名称
——
中文别名
——
英文名称
ethyl 2-(3-fluoro-4-hydroxyphenyl)acetate
英文别名
(3-fluoro-4-hydroxy-phenyl)-acetic acid ethyl ester;(3-fluoro-4-hydroxyphenyl)acetic acid ethyl ester;ethyl (3-fluoro-4-hydroxyphenyl)acetate
ethyl 2-(3-fluoro-4-hydroxyphenyl)acetate化学式
CAS
259543-80-1
化学式
C10H11FO3
mdl
——
分子量
198.194
InChiKey
RVEGFWRETOTMRC-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):
    1.8
  • 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:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    4

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

  • 作为反应物:
    描述:
    ethyl 2-(3-fluoro-4-hydroxyphenyl)acetate 在 sodium azide 、 四丁基溴化铵 、 sodium hydride 、 potassium carbonate 、 potassium iodide 作用下, 以 N,N-二甲基甲酰胺丙酮甲苯 为溶剂, 反应 7.0h, 生成 ethyl 2-(4-(2-azidoethoxy)-3-fluorophenyl)propanoate
    参考文献:
    名称:
    The SAR analysis of TRPV1 agonists with the α-methylated B-region
    摘要:
    A series of TRPV1 agonists with amide, reverse amide, and thiourea groups in the B-region and their corresponding alpha-methylated analogues were investigated. Whereas the alpha-methylation of the amide B-region enhanced the binding affinities and potencies as agonists, that of the reverse amide and thiourea led to a reduction in receptor affinity. The analysis indicated that proper hydrogen bonding as well as steric effects in the B-region are critical for receptor binding. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.06.059
  • 作为产物:
    描述:
    3-氟-4-羟基苯乙酸盐酸乙醇 作用下, 反应 3.0h, 以99%的产率得到ethyl 2-(3-fluoro-4-hydroxyphenyl)acetate
    参考文献:
    名称:
    WO2008/46598
    摘要:
    公开号:
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文献信息

  • [EN] COMPOUNDS AND METHODS<br/>[FR] COMPOSÉS ET MÉTHODES
    申请人:TEMPERO PHARMACEUTICALS INC
    公开号:WO2013019682A1
    公开(公告)日:2013-02-07
    The present invention relates to novel retinoid-related orphan receptor gamma (RORγ) modulators and their use in the treatment of diseases mediated by RORy.
    本发明涉及新型视黄醛酸相关孤儿受体γ(RORγ)调节剂及其在治疗由RORγ介导的疾病中的应用。
  • [EN] PYRAZOLE COMPOUNDS AND THEIR USE AS T-TYPE CALCIUM CHANNEL BLOCKERS<br/>[FR] COMPOSÉS DE PYRAZOLE ET LEUR UTILISATION EN TANT QUE BLOQUEURS DES CANAUX CALCIQUES DE TYPE T
    申请人:ACTELION PHARMACEUTICALS LTD
    公开号:WO2015186056A1
    公开(公告)日:2015-12-10
    The invention relates to compounds of formula (I) Formula (I) wherein X, Y, R1, R2, (R4)n, and (R5)m are as defined in the description, and to pharmaceutically acceptable salts of such compounds. These compounds are useful as calcium T-channel blockers.
    这项发明涉及式(I)的化合物。式(I)中X、Y、R1、R2、(R4)n和(R5)m的定义如描述中所述,并且涉及这些化合物的药用盐。这些化合物可用作钙T通道阻滞剂。
  • Indoline derivatives
    申请人:Dittrich-Wengenroth Elke
    公开号:US20070197626A1
    公开(公告)日:2007-08-23
    The present invention relates to novel indoline derivatives, to processes for their preparation and to their use in medicaments, in particular as potent PPAR-delta-activating compounds for the prophylaxis and/or treatment of cardiovascular disorders, in particular of dyslipidaemias, arteriosclerosis and coronary heart diseases.
    本发明涉及新型吲哚啉衍生物,以及它们的制备过程和在药物中的应用,特别是作为强效PPAR-δ激活化合物,用于预防和/或治疗心血管疾病,特别是血脂异常、动脉硬化和冠心病。
  • [EN] THERAPEUTIC METHODS<br/>[FR] MÉTHODES THÉRAPEUTIQUES
    申请人:GLAXO GROUP LTD
    公开号:WO2013085890A1
    公开(公告)日:2013-06-13
    The present invention relates to methods of treatment of diseases mediated by RORϒ.
    本发明涉及通过RORϒ介导的疾病治疗方法。
  • Selective Estrogen Receptor Modulator
    申请人:Hamaoka Shinichi
    公开号:US20120004315A1
    公开(公告)日:2012-01-05
    The present invention provides a compound represented by the following formula (I); [wherein T represents a single bond, a C1-C4 alkylene group which may have a substituent and the like; formula (I-1) represents a single bond or a double bond; A represents a single bond, a bivalent 5- to 14-membered heterocyclic group which may have a substituent and the like; Y represents a single bond and the like; Z represents a methylene group and the like; ring G represents a phenylene group and the like which may condense with a 5- to 6-membered ring and may have a heteroatom; R a and R b are the same as or different from each other and represent a hydrogen atom and the like; W represents a single bond and the like; R′ represents 1 to 4 independent hydrogen atoms and the like; and R″ represents 1 to 4 independent hydrogen atoms and the like] or a salt thereof, or a hydrate thereof.
    本发明提供一种由以下式(I)表示的化合物; [其中T表示单键,可能具有取代基的C1-C4烷基和类似物;式(I-1)表示单键或双键;A表示单键,可能具有取代基的双价5-至14-成员杂环基和类似物;Y表示单键和类似物;Z表示亚甲基基团和类似物;环G表示苯基团和类似物,可能与5-至6-成员环缩合并可能具有杂原子;Ra和Rb相同或不同,表示氢原子和类似物;W表示单键和类似物;R'表示1到4个独立的氢原子和类似物;R''表示1到4个独立的氢原子和类似物]或其盐或水合物。
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