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4-hydroxy-4'-cyclohexyl-1,1'-biphenyl

中文名称
——
中文别名
——
英文名称
4-hydroxy-4'-cyclohexyl-1,1'-biphenyl
英文别名
4-cyclohexyl-4'-hydroxybiphenyl;4-(4-Cyclohexylphenyl)phenol
4-hydroxy-4'-cyclohexyl-1,1'-biphenyl化学式
CAS
——
化学式
C18H20O
mdl
——
分子量
252.356
InChiKey
JZYRYKFMJSKSMB-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):
    5.8
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-hydroxy-4'-cyclohexyl-1,1'-biphenyl三氟甲磺酸酐 作用下, 以 吡啶 为溶剂, 反应 24.0h, 以77.7%的产率得到4'-cyclohexylbiphenyl-4-yl trifluoromethanesulfonate
    参考文献:
    名称:
    Polymerizable compound, polymerizable resin composition, cured polymer and liquid crystal display device
    摘要:
    这项发明的可聚合化合物由通式(I)表示:其中R为H,R′,R′O,R′COO或R′OCO,R′为具有1至约15个碳原子的直链或支链烷基或烯基基团,A1和A2分别为环己烷环或苯环,可能包括下面通式(II)表示的取代基;X为H或CH3;Y1、Y2、Y3和Y4独立地为H、F、Cl、CH3、CH3O、CF3或CF3O,其中至少两个Y1、Y2、Y3和Y4为H,如果A1和A2均为环己烷环,则至少有一个Y1、Y2、Y3和Y4不为H:其中Y5、Y6、Y7和Y8独立地为H、F、Cl、CH3、CH3O、CF3或CF3O,至少两个Y5、Y6、Y7和Y8为H。
    公开号:
    US06388146B1
  • 作为产物:
    描述:
    对羟基联苯环己烯 为溶剂, 以86.7%的产率得到4-hydroxy-4'-cyclohexyl-1,1'-biphenyl
    参考文献:
    名称:
    Alkylation of aromatic compounds to alkylates enriched in the
    摘要:
    芳香化合物,如苯或联苯,与具有一至八个碳原子的烷基化剂(如丙烯)在酸性莫来石沸石催化剂的存在下烷基化,在足以产生富含线性烷基化异构体的取代芳香化合物混合物的条件下进行,例如对二异丙基苯或对,对' 二(异丙基)联苯。这种新型酸性莫来石催化剂的特征在于其硅铝摩尔比、孔隙度和对称指数。芳香化合物的对,对' 二取代异构体在制备热致液晶聚合物的单体中是有用的。
    公开号:
    US05004841A1
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文献信息

  • Alkylation of polycyclic aromatic compounds to alkylates enriched in the
    申请人:The Dow Chemical Company
    公开号:US04891448A1
    公开(公告)日:1990-01-02
    Polycyclic aromatic compounds, such as biphenyl, are alkylated with an alkylating agent, such as propylene, in the presence of an acidic mordenite zeolite catalyst under conditions sufficient to produce a mixture of substituted polycyclic aromatic compounds enriched in the para alkylated isomers, such as p,p'-di(isopropyl)biphenyl. The novel acidic mordenite catalyst is characterized by its silica/alumina molar ratio, its porosity, and a Symmetry Index. The p,p'-disubstituted isomers of polycyclic aromatic compounds are useful as monomers in the preparation of thermotropic, liquid crystal polymers.
    多环芳烃化合物,如联苯,与烷基化剂,如丙烯,在酸性莫来石沸石催化剂的存在下进行烷基化反应,条件足以产生富集于对位烷基化异构体的取代多环芳烃混合物,如p,p'-二(异丙基)联苯。这种新型酸性莫来石催化剂的特征在于其硅铝摩尔比、孔隙度和对称指数。多环芳烃化合物的p,p'-二取代异构体在制备热致液晶聚合物的单体中是有用的。
  • Alkylation of polycyclic aromatic compounds to alkylates enriched in the para-substituted isomers
    申请人:THE DOW CHEMICAL COMPANY
    公开号:EP0317907A2
    公开(公告)日:1989-05-31
    Aromatic compounds, such as benzene or biphenyl, are alkylated with an alkylating agent, such as propylene, in the presence of an acidic mordenite zeolite catalyst under conditions sufficient to produce a mixture of substituted polycyclic aromatic compounds enriched in the para alkylated isomers, such as p-­diisopropyl-benzene or p,p′-di(isopropyl)biphenyl, respectively. The novel acidic mordenite catalyst is characterized by its silica/alumina molar ratio, its porosity, and Symmetry Index. The p,p′-disubstituted isomers of aromatic compounds are useful as monomers in the preparation of thermotropic, liquid crystal polymers.
    芳香族化合物(如苯或联苯)在酸性莫代沸石催化剂存在下与烷化剂(如丙烯)发生烷基化反应,其条件足以生成富含对位烷基化异构体的取代多环芳香族化合物混合物,如对二异丙基苯或对,p′-二(异丙基)联苯。新型酸性莫来石催化剂的特征在于其二氧化硅/氧化铝摩尔比、孔隙率和对称指数。芳香族化合物的对,对′-二取代异构体可用作制备热致性液晶聚合物的单体。
  • POLYMERIZABLE LIQUID CRYSTAL COMPOUND, LIQUID CRYSTAL COMPOSITION, OPTICAL ANISOTROPIC MATERIAL AND OPTICAL ELEMENT
    申请人:KAIDA Yuriko
    公开号:US20070104894A1
    公开(公告)日:2007-05-10
    To provide a novel compound which satisfies characteristics required for an optical anisotropic material and which is excellent in durability against blue laser light, a liquid crystal composition containing the compound, an optical anisotropic material employing the liquid crystal composition and an optical element. A compound represented by the following formula (1): CH 2 ═CR 1 —COO—(L) k -E 1 -E 2 -E 3 -(E 4 ) m -(E 5 ) n -R 2 (1) provided that the symbols in the formula have the following meanings: R 1 : a hydrogen atom or a methyl group; R 2 : a C 1-8 alkyl group; L: —(CH 2 ) p O—, —(CH 2 ) q —, -Cy-COO— (Cy is a trans-1,4-cyclohexylene group), -Cy-OCO—, -E 6 -(CH 2 ) 2 —, -E 7 -CH 2 O— or -E 8 -O— (wherein each of p and q which are independent of each other, is an integer of from 2 to 8); E 1 , E 2 , E 3 E 4 , E 5 , E 6 , E 7 , E 8 : each independently a 1,4-pheneylene group or a trans-1,4-cyclohexylene group (provided that at least one of E 1 , E 2 and E 3 is a trans-1,4-cyclohexylene group, and in a case where L is -Cy-OCO—, E 1 is a trans-1,4-cyclohexylene group), provided that the above 1,4-phenylene group and trans-1,4-cyclohexylene group may be such that a hydrogen atom bonded to a carbon atom in each group may be substituted by a fluorine atom, a chlorine atom or a methyl group; and k, m, n: each independently 0 or 1, provided that when k is 1 and L is -Cy-COO—, -Cy-OCO—, -E 6 -(CH 2 ) 2 —, -E 7 -CH 2 O— or -E 8 -O—, at least one of m and n is 0.
  • US4891448A
    申请人:——
    公开号:US4891448A
    公开(公告)日:1990-01-02
  • US5004841A
    申请人:——
    公开号:US5004841A
    公开(公告)日:1991-04-02
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