2,6-bis(methoxymethoxy)phenol | 1255188-42-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 2,6-bis(methoxymethoxy)phenol
• 英文别名: 2,6-Bis(methoxymethoxy)phenol
• CAS: 1255188-42-1
• 化学式: C₁₀H₁₄O₅
• 分子量: 214.218
• InChiKey: AMDRSNFHGUJDTD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  15
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  57.2
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2,6-bis(methoxymethoxy)phenol 、 氯乙酸甲酯 在 potassium carbonate 、 potassium iodide 作用下， 以 丙酮 为溶剂， 反应 13.0h， 以74%的产率得到methyl 2-(2,6-bis(methoxymethoxy)phenoxy)acetate
  参考文献：
  名称：

  Structure–activity relationships in 1,4-benzodioxan-related compounds. 10. Novel α1-adrenoreceptor antagonists related to openphendioxan: Synthesis, biological evaluation, and α1d computational study

  摘要：

  A series of novel openphendioxan analogues were synthesized and tested at alpha(1)-adrenoreceptor (AR) subtypes by binding and functional assays. The alpha(1d)-AR binding profile was also examined by means of 2D, 3D-QSAR together with docking studies. Multiple regression analysis suggested the relevance of adequate number of heteroatoms in the whole molecule and of passive membrane diffusion to enhance alpha(1d)-AR affinity. Docking simulations against a computational structural model of the biological target further proved this evidence and furnished support for chemiometric analysis, where polar, electrostatic, hydrophobic and shape effects of the ortho substituents in the phenoxy terminal, most likely governing ligand binding, helped the depiction of pharmacophore hypothesis for the examined ligands data set. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.08.002
• 作为产物：
  描述：

  1,3-双(甲氧基甲氧基)苯 在 正丁基锂 、 硼酸三甲酯 、 Oxone 、 碳酸氢钠 作用下， 以 四氢呋喃 、 水 、 丙酮 为溶剂， 反应 1.5h， 以33%的产率得到2,6-bis(methoxymethoxy)phenol
  参考文献：
  名称：

  Structure–activity relationships in 1,4-benzodioxan-related compounds. 10. Novel α1-adrenoreceptor antagonists related to openphendioxan: Synthesis, biological evaluation, and α1d computational study

  摘要：

  A series of novel openphendioxan analogues were synthesized and tested at alpha(1)-adrenoreceptor (AR) subtypes by binding and functional assays. The alpha(1d)-AR binding profile was also examined by means of 2D, 3D-QSAR together with docking studies. Multiple regression analysis suggested the relevance of adequate number of heteroatoms in the whole molecule and of passive membrane diffusion to enhance alpha(1d)-AR affinity. Docking simulations against a computational structural model of the biological target further proved this evidence and furnished support for chemiometric analysis, where polar, electrostatic, hydrophobic and shape effects of the ortho substituents in the phenoxy terminal, most likely governing ligand binding, helped the depiction of pharmacophore hypothesis for the examined ligands data set. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.08.002

文献信息

• Core-to-core dimers forming switchable mesophase
  作者：M. Horčic、J. Svoboda、V. Novotná、D. Pociecha、E. Gorecka

  DOI：10.1039/c6cc09983a

  日期：——

  We report structurally new type of dimers composed of bent-core molecules connected through their central cores by an alkylene spacer.

  我们报告了由弯曲核心分子通过烷基间隔连接它们的中心核心而组成的新型二聚体。
• Structure–activity relationships in 1,4-benzodioxan-related compounds. 10. Novel α1-adrenoreceptor antagonists related to openphendioxan: Synthesis, biological evaluation, and α1d computational study
  作者：Antonio Carrieri、Alessandro Piergentili、Fabio Del Bello、Mario Giannella、Maria Pigini、Amedeo Leonardi、Francesca Fanelli、Wilma Quaglia

  DOI：10.1016/j.bmc.2010.08.002

  日期：2010.10

  A series of novel openphendioxan analogues were synthesized and tested at alpha(1)-adrenoreceptor (AR) subtypes by binding and functional assays. The alpha(1d)-AR binding profile was also examined by means of 2D, 3D-QSAR together with docking studies. Multiple regression analysis suggested the relevance of adequate number of heteroatoms in the whole molecule and of passive membrane diffusion to enhance alpha(1d)-AR affinity. Docking simulations against a computational structural model of the biological target further proved this evidence and furnished support for chemiometric analysis, where polar, electrostatic, hydrophobic and shape effects of the ortho substituents in the phenoxy terminal, most likely governing ligand binding, helped the depiction of pharmacophore hypothesis for the examined ligands data set. (C) 2010 Elsevier Ltd. All rights reserved.