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4-(3-Amino-benzofuran-2-yl)-7-chloro-chromen-2-one | 863288-74-8

中文名称
——
中文别名
——
英文名称
4-(3-Amino-benzofuran-2-yl)-7-chloro-chromen-2-one
英文别名
4-(3-amino-1-benzofuran-2-yl)-7-chlorochromen-2-one
4-(3-Amino-benzofuran-2-yl)-7-chloro-chromen-2-one化学式
CAS
863288-74-8
化学式
C17H10ClNO3
mdl
——
分子量
311.724
InChiKey
AKDVTRRXRDIDTQ-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:
    526.6±50.0 °C(Predicted)
  • 密度:
    1.481±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.44
  • 重原子数:
    22.0
  • 可旋转键数:
    1.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    69.37
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    4-(3-Amino-benzofuran-2-yl)-7-chloro-chromen-2-one原乙酸三乙酯 生成 3-Chloro-7-methyl-5,13-dioxa-8-aza-indeno[1,2-c]phenanthren-6-one
    参考文献:
    名称:
    Synthesis and biological evaluation of novel angularly fused polycyclic coumarins
    摘要:
    In a three-step sequence, an array of angularly fused polycyclic heterocycles with coumarin, benzofuran and pyridine rings were synthesized from 4-bromomethylcoumarins and salicylonitrile. All the final compounds were fully characterized and screened for anti-microbial, anti-inflammatory and analgesic activities. Several compounds exhibited promising inflammation inhibiting and anti-microbial properties. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.05.063
  • 作为产物:
    参考文献:
    名称:
    Synthesis and biological evaluation of novel angularly fused polycyclic coumarins
    摘要:
    In a three-step sequence, an array of angularly fused polycyclic heterocycles with coumarin, benzofuran and pyridine rings were synthesized from 4-bromomethylcoumarins and salicylonitrile. All the final compounds were fully characterized and screened for anti-microbial, anti-inflammatory and analgesic activities. Several compounds exhibited promising inflammation inhibiting and anti-microbial properties. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.05.063
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