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3-bromo-2'-hydroxy-4-methoxychalcone | 1148010-40-5

中文名称
——
中文别名
——
英文名称
3-bromo-2'-hydroxy-4-methoxychalcone
英文别名
(E)-3-(3-bromo-4-methoxyphenyl)-1-(2-hydroxyphenyl)prop-2-en-1-one;(2E)-3-(3-bromo-4-methoxyphenyl)-1-(2-hydroxyphenyl)prop-2-en-1-one
3-bromo-2'-hydroxy-4-methoxychalcone化学式
CAS
1148010-40-5
化学式
C16H13BrO3
mdl
——
分子量
333.181
InChiKey
KXSKRIQLDQIBNJ-SOFGYWHQSA-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:
    20
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    3-bromo-2'-hydroxy-4-methoxychalcone 在 palladium 10% on activated carbon 、 氢气 作用下, 反应 3.0h, 以87%的产率得到3-(3-bromo-4-methoxyphenyl)-1-(2-hydroxyphenyl)propan-1-one
    参考文献:
    名称:
    Microwave-assisted synthesis of macrocycles via intramolecular and/or bimolecular Ullmann coupling
    摘要:
    Microwave-assisted synthesis of macrocyclic diaryl ethers via intramolecular and/or bimolecular Ullmann coupling is described. Using the optimized conditions, a panel of macrocycles, with different substitution patterns, ring sizes, and linkers, has been successfully synthesized using microwave irradiation. To the best of our knowledge, this work represents the first examples of the microwave-assisted synthesis of macrocyclic diaryl ethers via intramolecular and/or bimolecular Ullmann coupling. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.05.142
  • 作为产物:
    描述:
    3-溴-4-甲氧基苯甲醛2'-羟基苯乙酮 在 sodium hydroxide 作用下, 以 乙醇 为溶剂, 以67%的产率得到3-bromo-2'-hydroxy-4-methoxychalcone
    参考文献:
    名称:
    Microwave-assisted synthesis of macrocycles via intramolecular and/or bimolecular Ullmann coupling
    摘要:
    Microwave-assisted synthesis of macrocyclic diaryl ethers via intramolecular and/or bimolecular Ullmann coupling is described. Using the optimized conditions, a panel of macrocycles, with different substitution patterns, ring sizes, and linkers, has been successfully synthesized using microwave irradiation. To the best of our knowledge, this work represents the first examples of the microwave-assisted synthesis of macrocyclic diaryl ethers via intramolecular and/or bimolecular Ullmann coupling. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.05.142
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文献信息

  • Inhibitory activity of prostaglandin E2 production by the synthetic 2′-hydroxychalcone analogues: Synthesis and SAR study
    作者:Thanh-Dao Tran、Haeil Park、Hyun Pyo Kim、Gerhard F. Ecker、Khac-Minh Thai
    DOI:10.1016/j.bmcl.2009.02.001
    日期:2009.3
    A series of 2'-hydroxychalcones has been synthesized and screened for their in vitro inhibitory activities of cyclooxygenase-2 catalyzed prostaglandin production from lipopolysaccharide-treated RAW 264.7 cells. Structure-activity relationship study suggested that inhibitory activity against prostaglandin E-2 production was governed to a greater extent by the substituent on B ring of the chalcone, and most of the active compounds have at least two methoxy or benzyloxy groups on B ring. The relationship between chalcone structures and their PGE(2) inhibitory activities was also interpreted by docking study on cyclooxygenase-2. (C) 2009 Elsevier Ltd. All rights reserved.
  • Microwave-assisted synthesis of macrocycles via intramolecular and/or bimolecular Ullmann coupling
    作者:Li Shen、Charles J. Simmons、Dianqing Sun
    DOI:10.1016/j.tetlet.2012.05.142
    日期:2012.8
    Microwave-assisted synthesis of macrocyclic diaryl ethers via intramolecular and/or bimolecular Ullmann coupling is described. Using the optimized conditions, a panel of macrocycles, with different substitution patterns, ring sizes, and linkers, has been successfully synthesized using microwave irradiation. To the best of our knowledge, this work represents the first examples of the microwave-assisted synthesis of macrocyclic diaryl ethers via intramolecular and/or bimolecular Ullmann coupling. (C) 2012 Elsevier Ltd. All rights reserved.
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