6-(trans-4-Propylcyclohexyl)-2-naphthol | 79861-37-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 6-(trans-4-Propylcyclohexyl)-2-naphthol
• 英文别名: 6-(trans-4-propylcyclohexyl)naphthalene-2-ol
• CAS: 79861-37-3
• 化学式: C₁₉H₂₄O
• 分子量: 268.399
• InChiKey: IOIPFCQWKLBXEJ-SHTZXODSSA-N

物化性质

• 沸点：
  430.0±14.0 °C(Predicted)
• 密度：
  1.043±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.62
• 重原子数：
  20.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  20.23
• 氢给体数：
  1.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  6-(trans-4-Propylcyclohexyl)-2-naphthol 在 磺酰氯 、 potassium carbonate 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 15.0h， 生成
  参考文献：
  名称：

  JP5962949

  摘要：

  公开号：
• 作为产物：
  描述：

  6-(trans-4-n-propylcyclohexyl)-2-methoxy naphthalene 在 氢溴酸 、 溶剂黄146 作用下， 以 水 为溶剂， 生成 6-(trans-4-Propylcyclohexyl)-2-naphthol
  参考文献：
  名称：

  Naphthalene derivative and liquid crystal composition comprising the same

  摘要：

  本公开了一种新型液晶化合物，它是一种萘衍生物，可用作电光液晶显示材料，包含这种萘衍生物的液晶组合物以及包括它们的液晶显示装置。本发明提供的萘衍生物表现出优异的液晶性能，并且与目前广泛使用的液晶组合物或配方具有良好的相溶性。添加萘衍生物可以显著降低液晶组合物的阈值电压，同时保持其高响应速度。本发明的萘衍生物具有较大的双折射指数。此外，大多数本发明的萘衍生物分子中没有强极性基团，因此也可用于有源矩阵驱动。此外，如前述示例所示，本发明的萘衍生物易于生产，无色且化学稳定。因此，包括本发明的萘衍生物的液晶组合物非常有用，特别是在广泛温度范围内运行且需要高速响应和低电压驱动的液晶组合物。

  公开号：

  US06468607B1

文献信息

• SYNTHESIS OF VICINAL DIFLUORO AROMATICS AND INTERMEDIATES THEREOF
  申请人：——

  公开号：US20020099247A1

  公开（公告）日：2002-07-25

  A method of preparing vicinal difluoro aromatic compounds in high yield from hydroxy aromatic compounds and a method of preparing intermediates thereof. The hydroxy aromatic compound can be a mono-, bi- or tricyclic aromatic in which the rings are separate or fused. One or more of the rings can contain heteroatoms, such as oxygen, nitrogen, or sulfur, and can contain one or more substitutions, in addition to the hydroxy substitution.

  从羟基芳香化合物制备高收率的邻二氟芳香化合物的方法以及制备其中间体的方法。羟基芳香化合物可以是一个单环、双环或三环芳香化合物，其中环是分开的或融合的。一个或多个环可以含有杂原子，如氧、氮或硫，并且除了羟基取代外，还可以含有一个或多个取代基。
• Synthesis of vicinal difluoro aromatics and intermediates thereof
  申请人：——

  公开号：US20030149315A1

  公开（公告）日：2003-08-07

  A method of preparing vicinal difluoro aromatic compounds in high yield from hydroxy aromatic compounds using various bases and a method of preparing intermediates thereof. A method for making a vicinal difluoro halogenated aromatic compound including providing a tetrafluoro derivative of a halogen substituted aromatic compound, wherein the tetrafluoro derivative has two fluorine atoms on each of two adjacent carbons and at least one additional halogen substituent; reacting the tetrafluoro derivative with a reducing agent in presence of a base for a reaction time sufficient to form the vicinal difluoro halogenated aromatic compound containing two vicinal fluorine substituents and the at least one additional halogen substituent, wherein the reducing agent is used in a reducing agent effective amount sufficient to retain the at least one additional halogen substituent.

  一种从羟基芳香化合物中使用各种碱制备高产率邻二氟芳香化合物的方法，以及制备其中间体的方法。一种制备邻二氟卤代芳香化合物的方法，包括提供卤代芳香化合物的四氟衍生物，其中四氟衍生物在两个相邻碳上各有两个氟原子和至少一个额外的卤素取代基；将四氟衍生物与还原剂在碱的存在下反应，反应时间足以形成含有两个邻二氟氟取代基和至少一个额外卤素取代基的邻二氟卤代芳香化合物，其中还原剂用于还原剂有效量足以保留至少一个额外卤素取代基。
• Liquid crystalline naphthalene derivatives
  申请人：Merck Patent Gesellschaft mit beschrankter Haftung

  公开号：US04386007A1

  公开（公告）日：1983-05-31

  Liquid crystalline naphthalene derivatives of the formula ##STR1## wherein ring A is 1,4-phenylene, trans-1,4-cyclohexylene or 1,4-cyclohex-1-enylene and ring system BC is 2,6-naphthylene, 3,4-dihydro-2,6-naphthylene or 1,2,3,4-tetrahydro-2,6-naphthylene, with the proviso that A is not 1,4-phenylene when BC is 2,6-naphthylene; and R.sub.1 and R.sub.2, which are identical or different, are each alkyl of up to 8 C atoms or, when the rings to which they are bonded are aromatic, also can be alkoxy, alkanoyloxy or alkoxycarbonyloxy having up to 8 C atoms in each case; or one of R.sub.1 and R.sub.2 also can be CN, halogen, CF.sub.3 or NO.sub.2 are valuable components for liquid crystalline dielectrics.

  公式为 ##STR1## 的液晶萘衍生物，其中环A为1,4-苯基、反-1,4-环己基或1,4-环己-1-烯基，环系统BC为2,6-萘基、3,4-二氢-2,6-萘基或1,2,3,4-四氢-2,6-萘基，但当BC为2,6-萘基时，A不是1,4-苯基；R.sub.1和R.sub.2相同或不同，均为碳数不超过8的烷基，或当它们连接的环为芳香族时，也可以是烷氧基、烷酰氧基或烷氧羰基氧基，每种情况下均具有不超过8个碳原子；或R.sub.1和R.sub.2中的一个也可以是CN、卤素、CF.sub.3或NO.sub.2，是液晶介质的有价值组分。
• Design, Synthesis and Physical Properties of New Liquid Crystal Materials for Active Matrix LCD (2)
  作者：Makoto Negishi、Shinji Ogawa、Masashi Osawa、Tatsuo Kawara、Tetsuo Kusumoto、Kiyofumi Takeuchi、Sadao Takehara、Haruyoshi Takatsu

  DOI：10.1080/10587250108025059

  日期：2001.8

  Novel 1-fluoro- and 1,2-difluoronaphthalene derivatives were designed for active matrix LCD and were prepared through the regioselective fluorination of 6-substituted 2-naphthols. These compounds exhibited high nematic-isotropic transition temperatures with very large dielectric anisotropy and large birefringences. These results are useful for design of new liquid crystal mixtures for TFT-displays.
• Design, Synthesis and Physical Properties of New Liquid Crystal Materials Having a Fluoro-Substituted Tetrahydronaphthalene Structure for Active Matrix LCD
  作者：Tetsuo Kusumoto、Yoshitaka Saito、Yutaka Nagashima、Makoto Negishi、Sadao Takehara、Yoshinori Iwashita、Kiyofumi Takeuchi、Haruyoshi Takatsu、Corneria Pithart、Rainer Frings、Artur Lachowicz、Gerwald Grahe

  DOI：10.1080/15421400490434973

  日期：2004.1

  Liquid crystal materials having a fluoro-substituted tetralhydro-naphthalene structure were designed for active matrix LCD. 6-Aryl-5-fluoro-1,2,3,4-tetrahydronaphthalenes and 5,6-difluro-1,2,3,4-tetrahydronaphthalenes were prepared by regioselective fluorination and hydrogenation of 2-naphthols. 6-Aryl-5,7-difluoro-1,2,3,4-tetrahydronaphthalenes were synthesized from 5,7-difluoro-1,2,3,4-tetrahydronaphthalene-2-one. The liquid crystal mixture containing these compounds with very good co-solubility exhibits a wide nematic temperature range with low melting point and very large value of dielectric anisotropy. From these results these compounds are useful for design. of new liquid crystal mixtures for TFT-displays.