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1-(p-hydroxybenzyl)-2-naphthol | 4895-95-8

中文名称
——
中文别名
——
英文名称
1-(p-hydroxybenzyl)-2-naphthol
英文别名
1-(4-hydroxybenzyl)naphthalen-2-ol;1-[(4-Hydroxyphenyl)methyl]naphthalen-2-ol
1-(p-hydroxybenzyl)-2-naphthol化学式
CAS
4895-95-8
化学式
C17H14O2
mdl
——
分子量
250.297
InChiKey
DWZJXWARJZXIMU-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):
    4.4
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Facile synthesis of diarylmethanes via quinone methides
    摘要:
    A novel acid-mediated generation of quinone methides followed by nucleophilic addition of electron-rich aromatic compounds to furnish diarylmethanes has been developed. A wide range of electron-rich aromatic compounds including some heterocycles can be employed for this reaction to provide the corresponding diarylmethanes in good yields and regioselectivities. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.10.087
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文献信息

  • Bowman, Peter J.; Brown, Ben R.; Chapman, M. Andrew, Journal of Chemical Research, Miniprint, 1984, # 3, p. 701 - 770
    作者:Bowman, Peter J.、Brown, Ben R.、Chapman, M. Andrew、Doyle, Paul M.
    DOI:——
    日期:——
  • BOWMAN, P. J.;BROWN, B. R.;CHAPMAN, M. A.;DOYLE, P. M., J. CHEM. RES. MICROFICHE, 1984, N 3, 72-73
    作者:BOWMAN, P. J.、BROWN, B. R.、CHAPMAN, M. A.、DOYLE, P. M.
    DOI:——
    日期:——
  • Facile synthesis of diarylmethanes via quinone methides
    作者:Kassrin Tangdenpaisal、Wong Phakhodee、Somsak Ruchirawat、Poonsakdi Ploypradith
    DOI:10.1016/j.tet.2012.10.087
    日期:2013.1
    A novel acid-mediated generation of quinone methides followed by nucleophilic addition of electron-rich aromatic compounds to furnish diarylmethanes has been developed. A wide range of electron-rich aromatic compounds including some heterocycles can be employed for this reaction to provide the corresponding diarylmethanes in good yields and regioselectivities. (C) 2012 Elsevier Ltd. All rights reserved.
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