4-Phenoxy-benzoldiazonium-chlorid | 6099-72-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-Phenoxy-benzoldiazonium-chlorid
• 英文别名: 4-Phenoxybenzene-1-diazonium chloride；4-phenoxybenzenediazonium;chloride
• CAS: 6099-72-5
• 化学式: C₁₂H₉N₂O*Cl
• 分子量: 232.669
• InChiKey: FPXDOKLNQMNWSW-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  0.97
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  37.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-Phenoxy-benzoldiazonium-chlorid 在 sodium azide 作用下， 以 水 为溶剂， 反应 1.0h， 生成 1-azido-4-phenoxybenzene
  参考文献：
  名称：

  Parallel Synthesis of “Click” Chalcones as Antitubulin Agents

  摘要：

  研究表明，某些查耳酮能够抑制微管蛋白聚合，从而产生细胞毒性和破坏肿瘤血管。通过点击化学合成并筛选了180种新型查耳酮类似物，以评估其细胞毒性和微管组装抑制活性。在180种点击查耳酮中，有10种显示出低微摩尔级别的细胞毒性，但仅有化合物Nf表现出抗微管活性。尽管Nf仅显示出微摩尔级别的效力，但这一结果表明点击查耳酮可能作为抗微管剂，并验证了通过此策略寻找新活性化合物的方法。

  DOI：

  10.2174/1573406411309040004
• 作为产物：
  描述：

  4-氨基二苯醚 在 盐酸 、 sodium nitrite 作用下， 以 水 为溶剂， 反应 1.0h， 生成 4-Phenoxy-benzoldiazonium-chlorid
  参考文献：
  名称：

  新型针对琥珀酸脱氢酶的抗真菌药物的权宜之计：带有二苯醚片段的吡唑-4-甲酰肼衍生物

  摘要：

  含有柔性酰胺链的吡唑-4-羧酰胺支架已经成为靶向琥珀酸脱氢酶（SDH）的高效农业杀菌剂的分子骨架。基于上述琥珀酸脱氢酶抑制剂（SDHI）的重要结构特征，在生物活性分子与SDH之间的虚拟对接比较的指导下，合理构思了三种新型的带有联苯醚部分的吡唑-4-甲酰肼衍生物。与分子对接比较的虚拟验证结果一致，体外抗真菌生物测定表明，标题化合物的骨架结构应优化为N '-（4-苯氧基苯基）-1 H-吡唑-4-碳酰肼支架。惊人地N '-（4-苯氧基苯基）-1 H-吡唑-4-碳酰肼衍生物对solani solani的影响11o，对禾谷镰刀菌（Fusarium graminearum）的11m和对灰葡萄孢的11g表现出优异的抗真菌作用，相应的EC 50值为0.14、0.27和0.52 μg/ mL，明显优于多菌灵（针对多菌灵（0.34μg / mL）和禾本科镰刀菌（0.57μg/ mL））和戊硫吡拉（对灰霉病）（0

  DOI：

  10.1021/acs.jafc.0c03736

文献信息

• Method of preparing an inkjet ink imaged lithographic printing plate
  申请人：Kodak Polychrome Graphics, L.L.C.

  公开号：US20030007052A1

  公开（公告）日：2003-01-09

  The present invention includes a method of preparing an inkjet ink imaged lithographic printing plate, comprising the steps of: imagewise applying onto a substrate coated with an inkjet ink reactive coating composition comprising a diazonium material, an inkjet ink to produce an imaged coated substrate wherein the inkjet ink imaged regions are oleophilic and more developer-insoluble than non-imaged regions; and contacting said imaged and non-imaged regions of said an imaged coated substrate and an aqueous developer to selectively remove said coating from said developer soluble non-imaged regions. The present invention also includes a lithographic printing plate, such as an inkjet ink imaged lithographic printing plate, which is prepared by the method of the present invention.

  本发明包括一种制备喷墨墨水成像平版印刷版的方法，包括以下步骤：在涂有包含重氮材料的喷墨墨水活性涂层组合物的基板上成像地涂布喷墨墨水，以产生成像涂层基板，其中喷墨墨水成像区域比非成像区域亲油且更不溶于显影剂；以及将所述成像涂层基板的所述成像和非成像区域与水性显影剂接触，以选择性地从所述可溶于显影剂的非成像区域去除所述涂层。本发明还包括平版印刷版，例如喷墨墨水成像平版印刷版，它是通过本发明的方法制备的。
• Synthesis and biological activity of a novel class of pyridazine analogues as non-competitive reversible inhibitors of protein tyrosine phosphatase 1B (PTP1B)
  作者：C Liljebris

  DOI：10.1016/s0968-0896(02)00176-1

  日期：2002.10

  A series of novel pyridazine analogues were prepared and the structure activity relationship of their behavior as inhibitors of PTP1B was evaluated. Most of the analogues had potencies in the low micromolar range. The in vitro kinetics of this compound series demonstrated that they were reversible non-competitive binders. This indicates that there may exist another site in the enzyme through which enzyme activity can be inhibited, which is not a recognized interaction domain. Some of the analogues exhibited high selectivity for other PTPases, for example, compound 12mp showed 20-fold selectivity for PTP1B (IC50 = 5.6 muM) versus both TCPTP and LAR (>100 muM, respectively). In contrast to many tyrosine phosphatase mimetic inhibitors, this compound class lacks negative charge and thus showed high permeability across cell membranes. Selective analogues in the series were analyzed in an in vitro cellular assay, which showed increased insulin-stimulated insulin receptor phosphorylation. (C) 2002 Elsevier Science Ltd. All rights reserved.
• Substituent effects on13C and15N chemical shifts in triazenes studied by principal components multivariate data analysis
  作者：W. J. Dunn、C. Lins、G. Kumar、T. Manimaran、S. Grigoras、U. Edlund、S. Wold

  DOI：10.1002/omr.1270210710

  日期：1983.7

  AbstractPrincipal components analysis was applied to the 13C and 15N chemical shift data on a series of fifteen 1‐(para‐substituted‐phenyl)‐3‐acetyl‐3‐methyltriazenes. It was found that the halogen‐substituted triazenes formed a class, based on substituent effects, which was different from the remaining eleven triazenes. A one‐component model described the halogen class, whereas a two‐component model was necessary for a description of the second class. In the second class, substituents tended to cluster to form groups depending on their electronic character.
• Suworow et al., Doklady Akademii Nauk SSSR, 1955, vol. 101, p. 103,105
  作者：Suworow et al.

  DOI：——

  日期：——
• Synthesis of Novel Tryptamine and Azepinoindole Derivatives
  作者：Lajos Novák、Michel Hanania、Péter Kovács、János Rohály、Pál Kolonits、Csaba Szántay

  DOI：10.3987/com-97-7918

  日期：——

  A novel one-pot synthesis of azepinoindoles (9) via reaction of tryptamines (4) with formaldehyde is described. The scope and generality of this new procedure and the preparation of the starting compounds are also discussed.