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ethyl 6-chloro-7-(bromomethyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylate | 775329-84-5

中文名称
——
中文别名
——
英文名称
ethyl 6-chloro-7-(bromomethyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylate
英文别名
ethyl 7-(bromomethyl)-6-chloro-2-(trifluoromethyl)-2H-chromene-3-carboxylate
ethyl 6-chloro-7-(bromomethyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylate化学式
CAS
775329-84-5
化学式
C14H11BrClF3O3
mdl
——
分子量
399.592
InChiKey
ISWJINXQQOJMHB-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):
    4.5
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    6

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

  • Benzopyran compounds useful for treating inflammatory conditions
    申请人:Carter Jeffery
    公开号:US20050148777A1
    公开(公告)日:2005-07-07
    The subject invention concerns methods and compounds that have utility in the treatment of a condition associated with cyclooxygenase-2 mediated disorders. Compounds of particular interest are benzopyrans and their analogs defined by formula 1 Wherein Z, X, R 1 , R 2, R 3 , and R 4 are as described in the specification.
    本发明涉及与环氧合酶-2介导的疾病相关的病症治疗方法和化合物。特别感兴趣的化合物是由公式1定义的苯并喃和其类似物,其中Z、X、R1、R2、R3和R4如规范中所述。
  • Benzopyran compounds for use in the treatment and prevention of inflammation related conditions
    申请人:Carter Jeffery
    公开号:US20050148627A1
    公开(公告)日:2005-07-07
    The subject invention concerns methods and compounds that have utility in the treatment of a condition associated with cyclooxygenase-2 mediated disorders. Compounds of particular interest are benzopyrans and their analogs defined by formula 1 Wherein Z, X, R 1 , R 2 , R 3 , and R 4 are as described in the specification.
    本发明涉及用于治疗与环氧合酶-2介导的疾病相关的条件的方法和化合物。特别感兴趣的化合物是苯并喃和它们的类似物,其由公式1定义,其中Z、X、R1、R2、R3和R4如规范中所述。
  • The novel benzopyran class of selective cyclooxygenase-2 inhibitors. Part 2: The second clinical candidate having a shorter and favorable human half-life
    作者:Jane L. Wang、David Limburg、Matthew J. Graneto、John Springer、Joseph Rogier Bruce Hamper、Subo Liao、Jennifer L. Pawlitz、Ravi G. Kurumbail、Timothy Maziasz、John J. Talley、James R. Kiefer、Jeffery Carter
    DOI:10.1016/j.bmcl.2010.07.054
    日期:2010.12
    In this Letter, we provide the structure-activity relationships, optimization of design, testing criteria, and human half-life data for a series of selective COX-2 inhibitors. During the course of our structure-based drug design efforts, we discovered two distinct binding modes within the COX-2 active site for differently substituted members of this class. The challenge of a undesirably long human half-life for the first clinical candidate 1 t(1/2) = 360 h was addressed by multiple strategies, leading to the discovery of 29b-(S) (SC-75416) with t(1/2) = 34 h. (C) 2010 Elsevier Ltd. All rights reserved.
  • [EN] BENZOPYRAN COMPOUNDS USEFUL FOR TREATING INFLAMMATORY CONDITIONS<br/>[FR] COMPOSES BENZOPYRANIQUES UTILISABLES DANS LE TRAITEMENT DES PATHOLOGIES INFLAMMATOIRES
    申请人:PHARMACIA CORP
    公开号:WO2004087686A3
    公开(公告)日:2004-12-16
  • EP1615905A2
    申请人:——
    公开号:EP1615905A2
    公开(公告)日:2006-01-18
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