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4,4'-Dihydroxy-3,3'-diacetyl-biphenyl | 13938-28-8

中文名称
——
中文别名
——
英文名称
4,4'-Dihydroxy-3,3'-diacetyl-biphenyl
英文别名
4,4'-Dihydroxy-3,3'-diacetyl biphenyl;1-[5-(3-acetyl-4-hydroxyphenyl)-2-hydroxyphenyl]ethanone
4,4'-Dihydroxy-3,3'-diacetyl-biphenyl化学式
CAS
13938-28-8
化学式
C16H14O4
mdl
——
分子量
270.285
InChiKey
MHZOXWCTOKMKQK-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):
    3.3
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    74.6
  • 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
  • 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:
    4,4'-Dihydroxy-3,3'-diacetyl-biphenyl 、 sodium hydride 作用下, 以 四氢呋喃二甲基亚砜 、 mineral oil 为溶剂, 反应 25.25h, 生成 Bis-<2-(4-methoxyphenyl)-chromen-4-on-6-yl>
    参考文献:
    名称:
    Synthesis and antifungal activities of natural and synthetic biflavonoids
    摘要:
    The synthesis of some natural and synthetic biflavonoids was performed in good overall yields starting from readily available materials via high yielding aldol and Ullmann condensations. Some of these compounds, especially bichalcones, display an interesting activity against fungi, higher than that of the corresponding monomers. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2011.04.010
  • 作为产物:
    描述:
    4,4'-双乙酰联苯 在 aluminum (III) chloride 、 盐酸 作用下, 以 氯苯 为溶剂, 反应 8.0h, 以72%的产率得到4,4'-Dihydroxy-3,3'-diacetyl-biphenyl
    参考文献:
    名称:
    Synthesis and antifungal activities of natural and synthetic biflavonoids
    摘要:
    The synthesis of some natural and synthetic biflavonoids was performed in good overall yields starting from readily available materials via high yielding aldol and Ullmann condensations. Some of these compounds, especially bichalcones, display an interesting activity against fungi, higher than that of the corresponding monomers. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2011.04.010
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文献信息

  • The Preparation of Some New Alkylphenols<sup>1</sup>
    作者:R. W. Stoughton、R. Baltzly、A. Bass
    DOI:10.1021/ja01324a505
    日期:1934.9
  • Madhvi; Karia; Parsania, Journal of the Indian Chemical Society, 2009, vol. 86, # 6, p. 588 - 593
    作者:Madhvi、Karia、Parsania
    DOI:——
    日期:——
  • A novel biphenyl-derived salicylhydrazone Schiff base fluorescent probes for identification of Cu2+ and application in living cells
    作者:Yun-Shang Yang、Suo-Suo Ma、Ying-Peng Zhang、Jia-Xi Ru、Xiao-Yu Liu、Hui-Chen Guo
    DOI:10.1016/j.saa.2018.03.060
    日期:2018.6
    A novel biphenyl-derived salicylhydrazone Schiff base (BSS) fluorescent probes for highly sensitive and selective identification of Cu2+ has been synthesized. In addition, the recognition has been proved experimentally. The results indicated that the complex forms a 1:1 complex with Cu2+ shows fluorescent quenching. Furthermore, the detection limit of 1.54 x 10(-8) M. More interesting, the probe BSS not only have a good biocompatibility in living cells, but also the sense behavior of Cu2+ in the cell nucleus. (C) 2018 Elsevier B.V. All rights reserved.
  • Regioselective Tandem [4 + 1]–[4 + 2] Synthesis of Amino-Substituted Dihydroxanthones and Xanthones
    作者:Ana Bornadiego、Jesús Díaz、Carlos F. Marcos
    DOI:10.1021/acs.joc.5b00658
    日期:2015.6.19
    A highly convergent and operationally simple approach to mycotoxin-related 4-amino-substituted 1-hydroxy-dihydroxanthones is described. The target compounds are obtained in one pot by the multicomponent reaction of 3-carbonylchromones, isocyanides, and nonsymmetric dienophiles. The reaction, which involves a tandem [4 + 1]-[4 + 2] cydoaddition, efficiently affords a variety of both monomeric and dimeric polysubstituted dihydroxanthones structurally similar to bioactive ergochromes. Further aromatization to the corresponding xanthones is readily achieved by treatment with DBU under microwave irradiation.
  • Boon-Long, 1948, vol. 1, # 4, p. 5,9
    作者:Boon-Long
    DOI:——
    日期:——
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