1,4-Dihexyloxynaphthalene | 875628-02-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 1,4-Dihexyloxynaphthalene
• 英文别名: 1,4-bis(hexyloxy)-naphthalene；1,4-Dihexoxynaphthalene
• CAS: 875628-02-7
• 化学式: C₂₂H₃₂O₂
• 分子量: 328.495
• InChiKey: GLOFORNNCSOOBE-UHFFFAOYSA-N

物化性质

• 沸点：
  453.7±18.0 °C(Predicted)
• 密度：
  0.975±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  7.8
• 重原子数：
  24
• 可旋转键数：
  12
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1,4-Dihexyloxynaphthalene 在 sodium hydroxide 、 N-溴代丁二酰亚胺(NBS) 、 苄基三乙基氯化铵 、 苯基锂 作用下， 以 四氢呋喃 、 二氯甲烷 、 氯仿 、 水 为溶剂， 反应 24.0h， 生成 1,2,3,4-tetrafluoro-6,11-bis(hexyloxy)-tetracene
  参考文献：
  名称：

  Syntheses of Soluble, π-Stacking Tetracene Derivatives

  摘要：

  The syntheses of a series of fluorine- and alkyl/alkoxy-functionalized tetracenes are reported. These functional groups are found to improve the solubility in common organic solvents and tune molecular arrangement in solids. The crystal packing, electrochemical behavior, and UV-vis absorbance spectroscopy of these materials are discussed.

  DOI：

  10.1021/ol0526468
• 作为产物：
  描述：

  1,4-二羟基萘 、 1-碘己烷 在 18-冠醚-6 、 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 96.0h， 以21.3%的产率得到1,4-Dihexyloxynaphthalene
  参考文献：
  名称：

  Syntheses of Soluble, π-Stacking Tetracene Derivatives

  摘要：

  The syntheses of a series of fluorine- and alkyl/alkoxy-functionalized tetracenes are reported. These functional groups are found to improve the solubility in common organic solvents and tune molecular arrangement in solids. The crystal packing, electrochemical behavior, and UV-vis absorbance spectroscopy of these materials are discussed.

  DOI：

  10.1021/ol0526468

文献信息

• Martinez-Ruiz; Behnisch; Schweikart, Chemistry - A European Journal, 2000, vol. 6, # 8, p. 1294 - 1301
  作者：Martinez-Ruiz、Behnisch、Schweikart、Hanack、Lueer、Oelkrug

  DOI：——

  日期：——
• RADICAL POLYMERIZATION CONTROL AGENT AND RADICAL POLYMERIZATION CONTROL METHOD
  申请人：Kawasaki Kasei Chemicals Ltd.

  公开号：US20210122692A1

  公开（公告）日：2021-04-29

  A conventional polymerization inhibitor is for example an agent to scavenge radicals generated during storage of a radical polymerizable compound and used to stably handle the radical polymerizable compound, but is unnecessary when the radical polymerizable compound is to be subjected to radical polymerization reaction, and is preferably removed at the time of the radical polymerization reaction. The object of the present invention is to obviate inconvenience of removing the polymerization inhibitor at the time of radical polymerization. The radical polymerization control agent contained in a radical polymerizable composition of the present invention functions as a radical polymerization inhibitor for example stored in a dark place, but loses its radical polymerization inhibiting effect when polymerization is initiated while being irradiated with light at a certain specific wavelength at the time of polymerization. Thus, radical polymerization of the radical polymerizable compound is easily initiated without increasing the amount of a radical polymerization initiator. That is, the radical polymerization control agent of the present invention is a radical polymerization control agent which is a corn pound having an effect to inhibit radical polymerization of a radical polymerizable compound and which loses the radical polymerization inhibiting effect under irradiation with light rays containing light within a wavelength range of from 300 nm to 500 nm.