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4,4’-(1,3-金刚烷二基)二苯酚 | 37677-93-3

中文名称
4,4’-(1,3-金刚烷二基)二苯酚
中文别名
4,4-(1,3-金刚烷二基)二苯酚;4,4'-(1,3-金刚烷二基)二苯酚
英文名称
1,3-bis(4-hydroxyphenyl)adamantane
英文别名
1,3-Bis-(4-hydroxyphenyl)-adamantan;4,4'-(1,3-Adamantanediyl)bisphenol;4-[3-(4-hydroxyphenyl)-1-adamantyl]phenol
4,4’-(1,3-金刚烷二基)二苯酚化学式
CAS
37677-93-3
化学式
C22H24O2
mdl
——
分子量
320.431
InChiKey
DNLWYVQYADCTEU-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

物化性质

  • 熔点:
    200-202 °C (lit.)

计算性质

  • 辛醇/水分配系数(LogP):
    6.1
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

安全信息

  • WGK Germany:
    3
  • 海关编码:
    2907299090
  • 危险性防范说明:
    P501,P270,P264,P280,P302+P352,P337+P313,P305+P351+P338,P362+P364,P332+P313,P301+P312+P330
  • 危险性描述:
    H302,H315,H319
  • 储存条件:
    存放条件:室温、密封且干燥环境中。

SDS

SDS:d41d4c8e86cc5c99df1c2cd5dbcb058f
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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:
    4,4’-(1,3-金刚烷二基)二苯酚硝酸乙酸酐 作用下, 以 为溶剂, 反应 1.5h, 以70%的产率得到1,3-bis(4-hydroxy-3-nitrophenyl)adamantane
    参考文献:
    名称:
    EP1602641
    摘要:
    公开号:
  • 作为产物:
    描述:
    参考文献:
    名称:
    金刚烷基二氰酸酯的聚合动力学和所得聚合物的热性能
    摘要:
    首次通过常规和温度调制的 DSC 研究了基于金刚烷的二氰酸酯的液态聚合动力学。已经检测到聚合的后期阶段经历了从动力学控制到扩散控制的转变。对反应控制体系中聚合动力学的详细分析表明,在目前提出的自催化准一步模型的框架中可以很好地描述过程速率。所提出的模型消除了对初始转换值的任意猜测,这为广泛使用的截断 Sestak-Berggren 模型提供了合理的替代方案。与具有柔性烃桥接单元的二氰酸酯相比,基于金刚烷的二氰酸酯聚合产物表现出明显更高的热稳定性和玻璃化转变温度。获得的实验结果证实了我们关于氰酸酯分子的刚性对其反应性和相应聚合物产物的热性能影响的假设。
    DOI:
    10.1016/j.reactfunctpolym.2021.104956
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文献信息

  • Hydroxyphenyl adamantanes and process for the production of the same
    申请人:——
    公开号:US20030187307A1
    公开(公告)日:2003-10-02
    Hydroxyphenyl adamantanes are represented by the general formula (1): 1 wherein R is an alkyl group, cycloalkyl group or phenyl group; m is 0 or an integer 1 or 2; l is 0 or 1; when l is 1, hydroxy groups of substituted hydroxyphenyl groups at positions 1 and 3 are together in para-position; n is 0 or an integer 1, 2 or 3; and when l is 0, n is an integer 1, 2 or 3.
    羟基苯基重氮烷类化合物由通式(1)表示: 1 其中R为烷基、环烷基或苯基;m为0或整数1或2;l为0或1;当l为1时,取代羟基苯基的1和3位的羟基在对位上共同存在;n为0或整数1、2或3;当l为0时,n为整数1、2或3。
  • METHOD FOR PRODUCING CYANOGEN-HALIDE, CYANATE ESTER COMPOUND AND METHOD FOR PRODUCING THE SAME, AND RESIN COMPOSITION
    申请人:MITSUBISHI GAS CHEMICAL COMPANY, INC.
    公开号:US20150299110A1
    公开(公告)日:2015-10-22
    A method for efficiently producing a cyanogen halide with suppressed side effects, and a method for producing a high-purity cyanate ester compound at a high yield includes contacting a halogen molecule with an aqueous solution containing hydrogen cyanide and/or a metal cyanide, so that the hydrogen cyanide and/or the metal cyanide is allowed to react with the halogen molecule in the reaction solution to obtain the cyanogen halide, wherein more than 1 mole of the hydrogen cyanide or the metal cyanide is used based on 1 mole of the halogen molecule, and when an amount of substance of an unreacted hydrogen cyanide or an unreacted metal cyanide is defined as mole (A) and an amount of substance of the generated cyanogen halide is defined as mole (B), the reaction is terminated in a state in which (A):(A)+(B) is between 0.00009:1 and 0.2:1.
    一种用于高效生产抑制副作用的氰卤化物,以及以高收率生产高纯度氰酸酯化合物的方法包括将卤素分子与含有氢氰酸和/或金属氰化物的水溶液接触,使得氢氰酸和/或金属氰化物与卤素分子在反应溶液中发生反应以获得氰卤化物,其中基于1摩尔卤素分子使用超过1摩尔的氢氰酸或金属氰化物,当未反应的氢氰酸或未反应的金属氰化物的物质量定义为摩尔(A),生成的氰卤化物的物质量定义为摩尔(B),反应在(A):(A)+(B)介于0.00009:1和0.2:1之间的状态中终止。
  • Synthesis of Adamantane Aminoethers with Antitubercular Potential
    作者:Angeliki-Sofia Foscolos、Ioannis Papanastasiou、Andrew Tsotinis、Nicolas Kolocouris、George B. Foscolos、Anthony Vocat、Stewart T. Cole
    DOI:10.2174/1573406413666170125112709
    日期:2017.10.17
    b. METHOD A substituted diarylmethane moiety was introduced on the adamantane skeleton of the new derivatives. The synthesis of the above compounds involved the nucleophilic attack of the corresponding phenoxide, to the appropriate aminoalkylchloride hydrochloride under heating. RESULTS The double substituted adamantane derivatives with an aminoether side chain exhibit significant activity against
    背景技术由具有活性的1,2-乙二胺部分的氨基金刚烷衍生物是有前途的抗结核药这一事实引起了我们的兴趣,我们在此报道了N,N'-subspedd-4,4'-[adamantane-2 ,2-二基]双(苯氧基烷基胺)1a-g,N,N'-取代-4,4'-[金刚烷-1,3-二基]双(苯氧基烷基胺)2a-f,N,N'-取代-[4-(1-金刚烷基)苯氧基]烷基胺3a-d和N,N′-取代的-[4-(2-金刚烷基)-苯氧基]烷基胺4a,b。方法将取代的二芳基甲烷部分引入新衍生物的金刚烷骨架上。上述化合物的合成涉及相应的酚盐在加热下对适当的氨基烷基氯化物盐酸盐的亲核攻击。结果具有氨基醚侧链的双取代金刚烷衍生物对结核分枝杆菌表现出显着的活性。结论侧链氨基末端的长度和性质影响抗结核活性。金刚烷支架和氨基醚侧链被苯氧基和氮原子之间的三亚甲基间隔基进行双酚取代得到了更好的结果。(类比1f,g和2e,f)。这些发现值得
  • Cyanate ester compound, curable resin composition containing the same, and hardened product thereof
    申请人:MITSUBISHI GAS CHEMICAL COMPANY, INC.
    公开号:US09949369B2
    公开(公告)日:2018-04-17
    The present invention is a cyanate ester compound represented by the following formula (1): wherein Ar represents an aromatic ring; R1 each independently represents a hydrogen atom, an alkyl group, or an aryl group; n each independently represents an integer of 1 to 3; m+n is the same as the total number of hydrogen atoms in a monovalent aromatic group containing the aromatic ring and the hydrogen atoms; R2 represents a hydrogen atom (excluding a case where Ar represents a benzene ring; n each represents 1; R1 represents a hydrogen atom; m each represents 4, and a cyanate group is bonded to the benzene ring in the 4-position relative to an adamantyl group), or an alkyl group having 1 to 4 carbon atoms; and R3 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms.
    本发明是一种由下式(1)表示的氰酸酯化合物: 其中Ar代表芳香环;R1各自独立地代表氢原子、烷基或芳基;n各自独立地代表1到3的整数;m+n等于含有芳香环和氢原子的单价芳香基中氢原子的总数;R2代表氢原子(除非Ar代表苯环的情况;n各自代表1;R1代表氢原子;m各自代表4,并且氰酸酯基与苯环中的1,4-位置相对于一个莽丁基结合),或者具有1到4个碳原子的烷基;R3代表氢原子或具有1到4个碳原子的烷基。
  • 1,3-Bis(3-Formyl-4-Hydroxyphenyl)Adamantanes and Polynuclear Polyphenols Derived Therefrom
    申请人:Yoshitomo Akira
    公开号:US20080242896A1
    公开(公告)日:2008-10-02
    A new 1,3-bis(3-formyl-4-hydroxyphenyl)adamantane, which provides a material offering excellent properties such as heat resistance and mechanical strength for use as an intermediate material for adamantanebisphenol derivatives or use in photosensitive resist materials, epoxy resins and other synthetic resins, thermosensitive recording materials, and the like, can be obtained through an industrial process in an easy manner at a good yield and high purity by producing a Schiff base from a 1,3-bis(4-hydroxyphenyl)adamantane by causing it to react with a hexamethylenetetramine or other substance in the presence of an acid, and then hydrolyzing the obtained Schiff base using an acid. A new polynuclear polyphenol is also provided that may be derived from the same.
    一种新的1,3-双(3-甲醛基-4-羟基苯基)金刚烷,可作为金刚烷双酚衍生物的中间体材料或用于光敏感抗蚀材料、环氧树脂和其他合成树脂、热敏感记录材料等,具有优异的性能,如耐热性和机械强度。可以通过一个工业过程轻松获得这种材料,产率高,纯度高,方法是通过将1,3-双(4-羟基苯基)金刚烷与六亚甲基四胺或其他物质在酸的存在下发生反应,然后用酸水解得到的席夫碱。同时还提供了一种可能源自相同材料的新的多核多酚。
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