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6-Acetylamino-chroman-2-carboxylic acid | 847948-87-2

中文名称
——
中文别名
——
英文名称
6-Acetylamino-chroman-2-carboxylic acid
英文别名
6-acetamido-3,4-dihydro-2H-chromene-2-carboxylic acid
6-Acetylamino-chroman-2-carboxylic acid化学式
CAS
847948-87-2
化学式
C12H13NO4
mdl
——
分子量
235.24
InChiKey
MKZFHOJYJIXAOT-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

物化性质

  • 沸点:
    522.3±50.0 °C(Predicted)
  • 密度:
    1.362±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    75.6
  • 氢给体数:
    2
  • 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

反应信息

  • 作为反应物:
    描述:
    6-Acetylamino-chroman-2-carboxylic acid(2S,3s)-1-(2-甲基氨基-2-苯基-乙基)-吡咯烷-3-醇 在 O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate 作用下, 以 二氯甲烷 为溶剂, 生成 6-acetamido-N-((S)-2-((S)-3-hydroxypyrrolidin-1-yl)-1-phenylethyl)-N-methylchroman-2-carboxamide
    参考文献:
    名称:
    Potent and highly selective kappa opioid receptor agonists incorporating chroman- and 2,3-dihydrobenzofuran-based constraints
    摘要:
    Two novel chemical classes of kappa opioid receptor agonists, chroman-2-carboxamide derivatives and 2,3-dihydrobenzofuran-2-carboxamide derivatives, were synthesized. These agents exhibited high and selective affinity for the kappa opioid receptor. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.08.094
  • 作为产物:
    描述:
    苯并二氢吡喃-2-羧酸 在 palladium on activated charcoal 盐酸 、 lithium hydroxide 、 氢气硝酸三乙胺 作用下, 以 四氢呋喃甲醇 为溶剂, 生成 6-Acetylamino-chroman-2-carboxylic acid
    参考文献:
    名称:
    Potent and highly selective kappa opioid receptor agonists incorporating chroman- and 2,3-dihydrobenzofuran-based constraints
    摘要:
    Two novel chemical classes of kappa opioid receptor agonists, chroman-2-carboxamide derivatives and 2,3-dihydrobenzofuran-2-carboxamide derivatives, were synthesized. These agents exhibited high and selective affinity for the kappa opioid receptor. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.08.094
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文献信息

  • Fused bicyclic carboxamide derivatives and methods of their use
    申请人:Dolle E. Roland
    公开号:US20050054630A1
    公开(公告)日:2005-03-10
    Fused bicyclic carboxamide derivatives are disclosed. Pharmaceutical compositions containing the compounds and methods for their use are also disclosed.
    揭示了融合的双环羧酰胺衍生物。还公开了含有这些化合物的药物组合物以及它们的使用方法。
  • US7034051B2
    申请人:——
    公开号:US7034051B2
    公开(公告)日:2006-04-25
  • [EN] FUSED BICYCLIC CARBOXAMIDE DERIVATIVES AND METHODS OF THEIR USE<br/>[FR] DERIVES DE CARBOXAMIDES BICYCLIQUES FUSIONNES ET LEURS PROCEDES D'UTILISATION
    申请人:ADOLOR CORP
    公开号:WO2005023799A1
    公开(公告)日:2005-03-17
    Fused bicyclic carboxamide derivatives of the general formula (I) are disclosed. Pharmaceutical compositions containing the compounds and methods for their use, inter alia, in treating and/or preventing pain, pruritus, and gastrointestinal disorders are also disclosed.
  • Potent and highly selective kappa opioid receptor agonists incorporating chroman- and 2,3-dihydrobenzofuran-based constraints
    作者:Guo-Hua Chu、Minghua Gu、Joel A. Cassel、Serge Belanger、Thomas M. Graczyk、Robert N. DeHaven、Nathalie Conway-James、Mike Koblish、Patrick J. Little、Diane L. DeHaven-Hudkins、Roland E. Dolle
    DOI:10.1016/j.bmcl.2005.08.094
    日期:2005.12
    Two novel chemical classes of kappa opioid receptor agonists, chroman-2-carboxamide derivatives and 2,3-dihydrobenzofuran-2-carboxamide derivatives, were synthesized. These agents exhibited high and selective affinity for the kappa opioid receptor. (c) 2005 Elsevier Ltd. All rights reserved.
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