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ethyl (Z)-4-(9H-xanthen-9-yl)but-2-enoate | 403694-99-5

中文名称
——
中文别名
——
英文名称
ethyl (Z)-4-(9H-xanthen-9-yl)but-2-enoate
英文别名
——
ethyl (Z)-4-(9H-xanthen-9-yl)but-2-enoate化学式
CAS
403694-99-5
化学式
C19H18O3
mdl
——
分子量
294.35
InChiKey
QEOQBGZLFVBKGI-QPEQYQDCSA-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:
    399.5±21.0 °C(Predicted)
  • 密度:
    1.141±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 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

  • 作为反应物:
    描述:
    ethyl (Z)-4-(9H-xanthen-9-yl)but-2-enoate草酰氯 、 bis(N-tert-butylsalicylaldiminato)copper(II) 、 三甲基铝二异丁基氢化铝二甲基亚砜N,N-二甲基苯胺三乙胺lithium hexamethyldisilazane 作用下, 以 四氢呋喃甲醇二氯甲烷甲苯 为溶剂, 生成 (S)-((R)-2-Hydroxy-1-phenyl-ethylamino)-[(1S,2S,3R)-2-(morpholine-4-carbonyl)-3-(9H-xanthen-9-ylmethyl)-cyclopropyl]-acetonitrile
    参考文献:
    名称:
    Design, synthesis and preliminary evaluation of novel 3′-Substituted carboxycyclopropylglycines as antagonists at group 2 metabotropic glutamate receptors
    摘要:
    Two novel 3'-substituted carboxycylopropylglycines, (2S,1'S,2'S,3'R)-2-(3'- xanthenylmethyl-2'-carboxycyclopropyl)glycine (8a) and (2S,1'S,2'S,3'R)-2-(3'-xanthenylethyl-2'-carboxycyclopropyl)glycine (8b), were synthesized and evaluated as mGluR ligands. Compound 8b showed to be a potent group II antagonist with submicromolar activity. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(01)00656-4
  • 作为产物:
    描述:
    2-(9H-xanthen-9-yl)acetaldehyde 、 bis(trifluoroethyl)phosphonoacetate ethyl ester 在 18-冠醚-6双(三甲基硅烷基)氨基钾 作用下, 以 四氢呋喃 为溶剂, 以75%的产率得到ethyl (Z)-4-(9H-xanthen-9-yl)but-2-enoate
    参考文献:
    名称:
    Design, synthesis and preliminary evaluation of novel 3′-Substituted carboxycyclopropylglycines as antagonists at group 2 metabotropic glutamate receptors
    摘要:
    Two novel 3'-substituted carboxycylopropylglycines, (2S,1'S,2'S,3'R)-2-(3'- xanthenylmethyl-2'-carboxycyclopropyl)glycine (8a) and (2S,1'S,2'S,3'R)-2-(3'-xanthenylethyl-2'-carboxycyclopropyl)glycine (8b), were synthesized and evaluated as mGluR ligands. Compound 8b showed to be a potent group II antagonist with submicromolar activity. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(01)00656-4
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文献信息

  • Design, synthesis and preliminary evaluation of novel 3′-Substituted carboxycyclopropylglycines as antagonists at group 2 metabotropic glutamate receptors
    作者:Roberto Pellicciari、Gabriele Costantino、Maura Marinozzi、Antonio Macchiarulo、Laura Amori、Peter Josef Flor、Fabrizio Gasparini、Rainer Kuhn、Stephan Urwyler
    DOI:10.1016/s0960-894x(01)00656-4
    日期:2001.12
    Two novel 3'-substituted carboxycylopropylglycines, (2S,1'S,2'S,3'R)-2-(3'- xanthenylmethyl-2'-carboxycyclopropyl)glycine (8a) and (2S,1'S,2'S,3'R)-2-(3'-xanthenylethyl-2'-carboxycyclopropyl)glycine (8b), were synthesized and evaluated as mGluR ligands. Compound 8b showed to be a potent group II antagonist with submicromolar activity. (C) 2001 Elsevier Science Ltd. All rights reserved.
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