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2-(Benzyloxy)-4-hydroxybenzaldehyde | 1352526-75-0

中文名称
——
中文别名
——
英文名称
2-(Benzyloxy)-4-hydroxybenzaldehyde
英文别名
4-hydroxy-2-phenylmethoxybenzaldehyde
2-(Benzyloxy)-4-hydroxybenzaldehyde化学式
CAS
1352526-75-0
化学式
C14H12O3
mdl
——
分子量
228.247
InChiKey
OXGHTGSTZMSSRP-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):
    2.5
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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

反应信息

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文献信息

  • Unexpected copper mediated benzyl O→O migration during an Ullmann ether coupling
    作者:Corinne Vanucci-Bacqué、Slim Chaabouni、Isabelle Fabing、Florence Bedos-Belval、Michel Baltas
    DOI:10.1016/j.tetlet.2013.11.089
    日期:2014.1
    The synthesis of a highly functionalized phenolic diaryl ether 5,5'-oxybis(4-hydroxy-3-methoxybenzaldehyde) (1) potentially interesting as a new scaffold for drug design, has been carried out using Ullmann coupling conditions. An unusual benzyl migration in o-benzyloxyphenol moiety occurred during this reaction leading to an unexpected compound identified as 4-(benzyloxy)-3-(2-(benzyloxy)-4-formy1-6-methoxyphenoxy)-5-methoxy benzaldehyde (7). A rationale for this migration process is proposed. (C) 2013 Elsevier Ltd. All rights reserved.
  • Phenylazetidinone Derivatives
    申请人:Zimmer Daniel P.
    公开号:US20090005321A1
    公开(公告)日:2009-01-01
    Various azetidinone derivatives are described, as are pharmaceutical compositions containing these compounds and methods of treatment of diseases using these compounds. Other embodiments are also described.
  • WO2006/86562
    申请人:——
    公开号:——
    公开(公告)日:——
  • Macrocycle Dynamics in a Branched [8]Catenane Controlled by Three Different Stimuli in Three Different Regions
    作者:Antony Wing Hung Ng、Samuel Kin‐Man Lai、Chi‐Chung Yee、Ho Yu Au‐Yeung
    DOI:10.1002/anie.202110200
    日期:2022.1.3
    A branched [8]catenane was synthesized from a one-pot procedure with good efficiency. Rigidifying/loosening the mechanical bond in the core, middle or periphery of the [8]catenane resulted in, respectively a large, middle and small degree of change in the catenane dynamics and flexibility.
    支链 [8] 链烯是由一锅法合成的,效率很高。使 [8] 链的核心、中间或外围的机械键变硬/松动分别导致链动力学和柔性的大、中和小程度的变化。
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