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9-Bromo-3,7-dimethoxy-[1]benzofuro[3,2-b]chromen-11-one | 406214-63-9

中文名称
——
中文别名
——
英文名称
9-Bromo-3,7-dimethoxy-[1]benzofuro[3,2-b]chromen-11-one
英文别名
——
9-Bromo-3,7-dimethoxy-[1]benzofuro[3,2-b]chromen-11-one化学式
CAS
406214-63-9
化学式
C17H11BrO5
mdl
——
分子量
375.175
InChiKey
SMDPLZRJABPNIL-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):
    4.3
  • 重原子数:
    23
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    57.9
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 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:
    参考文献:
    名称:
    Constrained phytoestrogens and analogues as ERβ selective ligands
    摘要:
    A new series of ERbeta (ERbeta) selective ligands has been prepared. One of the compounds 6, structurally related to the phytoestrogen apigenin 4, displays a binding preference for ERbeta over ERalpha of over 40-fold. In addition to its binding selectivity, 6 was able to potently induce metallothionein (an ERbeta specific response in human SAOS-2 cells) while demonstrating low potency in an ERalpha dependant ERE-tk luciferase assay in MCF-7 cells. Such receptor and cell selectivity could make 6 a useful molecular probe for better understanding the role of ERbeta in mammalian physiology. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00394-9
  • 作为产物:
    描述:
    3-溴-2-羟基-5-甲氧基苯甲酸甲酯2-chloro-1-(2-fluoro-4,6-dimethoxy-phenyl)-ethanonecaesium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以65%的产率得到9-Bromo-3,7-dimethoxy-[1]benzofuro[3,2-b]chromen-11-one
    参考文献:
    名称:
    A highly efficient, one-pot synthesis of benzo[b]fluoren-10-ones
    摘要:
    5,[1-Dioxa- and 5-oxa-1]-thiabenzo[b]fluoren-10-ones were prepared via a one-pot procedure initiated by the reaction of salicylates or thiasalicylates with ortho fluoro-alpha -bromoacetophenones in the presence of cesium carbonate. The reactions proceeded in good yield and the final products were obtained without chromatography. The reaction presumably proceeds via a sequential intermolecular alkylation, intramolecular acylation sequence concluded by an intramolecular, ipso-fluoro substitution. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(01)01828-7
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文献信息

  • A highly efficient, one-pot synthesis of benzo[b]fluoren-10-ones
    作者:Michael D. Collini、Chris P. Miller
    DOI:10.1016/s0040-4039(01)01828-7
    日期:2001.11
    5,[1-Dioxa- and 5-oxa-1]-thiabenzo[b]fluoren-10-ones were prepared via a one-pot procedure initiated by the reaction of salicylates or thiasalicylates with ortho fluoro-alpha -bromoacetophenones in the presence of cesium carbonate. The reactions proceeded in good yield and the final products were obtained without chromatography. The reaction presumably proceeds via a sequential intermolecular alkylation, intramolecular acylation sequence concluded by an intramolecular, ipso-fluoro substitution. (C) 2001 Elsevier Science Ltd. All rights reserved.
  • Constrained phytoestrogens and analogues as ERβ selective ligands
    作者:Chris P Miller、Michael D Collini、Heather A Harris
    DOI:10.1016/s0960-894x(03)00394-9
    日期:2003.7
    A new series of ERbeta (ERbeta) selective ligands has been prepared. One of the compounds 6, structurally related to the phytoestrogen apigenin 4, displays a binding preference for ERbeta over ERalpha of over 40-fold. In addition to its binding selectivity, 6 was able to potently induce metallothionein (an ERbeta specific response in human SAOS-2 cells) while demonstrating low potency in an ERalpha dependant ERE-tk luciferase assay in MCF-7 cells. Such receptor and cell selectivity could make 6 a useful molecular probe for better understanding the role of ERbeta in mammalian physiology. (C) 2003 Elsevier Science Ltd. All rights reserved.
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