摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2',4',6'-trimethylbiphenyl-4-ol | 66818-64-2

中文名称
——
中文别名
——
英文名称
2',4',6'-trimethylbiphenyl-4-ol
英文别名
4-hydroxy-2',4',6'-trimethylbiphenyl;4’-hydroxy-2,4,6‑trimethyl-1-1'-biphenyl;2',4',6'-Trimethyl-4-biphenylol;4-(2,4,6-Trimethylphenyl)phenol
2',4',6'-trimethylbiphenyl-4-ol化学式
CAS
66818-64-2
化学式
C15H16O
mdl
——
分子量
212.291
InChiKey
FFUHDUUVERVMDP-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

  • 沸点:
    313.4±11.0 °C(Predicted)
  • 密度:
    1.051±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.3
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

上下游信息

  • 上游原料
    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:
    2',4',6'-trimethylbiphenyl-4-ol 、 2,3,4,6,7,8-Hexabromo-1,5-naphthyridine 在 正丁基锂 、 palladium diacetate 、 lithium tert-butoxide 、 tri tert-butylphosphoniumtetrafluoroborate 作用下, 以 邻二氯苯甲苯 为溶剂, 反应 30.0h, 生成
    参考文献:
    名称:
    有机化合物及显示面板
    摘要:
    本发明实施例公开了一种有机化合物及显示面板,该有机化合物具有如通式(1)所示的结构:#imgabs0#本发明通过使用具有多重共振效应的有机化合物,并通过拉长有机化合物中B和B之间的距离和/或引入N打断共轭减弱了对位电子耦合,改善了有机化合物的材料性能,从而提升了应用有机化合物的显示面板的发光效率、色纯度并延长了使用寿命。
    公开号:
    CN117720565A
  • 作为产物:
    参考文献:
    名称:
    Haefelinger,G. et al., Chemische Berichte, 1978, vol. 111, p. 1323 - 1329
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Nanocrystalline Titania-Supported Palladium(0) Nanoparticles for Suzuki-Miyaura Cross-Coupling of Aryl and Heteroaryl Halides
    作者:B. Sreedhar、Divya Yada、P. Surendra Reddy
    DOI:10.1002/adsc.201100012
    日期:2011.10
    The Suzuki cross-coupling reaction of various aryl and heteroaryl halides with arylboronic and heteroarylboronic acids was studied using a titania-supported palladium(0) catalyst at room temperature under air. The conversion and selectivity results obtained for many substrates were excellent and similar to those provided by more active or even homogeneous catalysts. The methodology is similarly effective
    使用二氧化钛负载的(0)催化剂在室温下于空气中研究了各种芳基和杂芳基卤化物与芳基硼酸和杂芳基硼酸的Suzuki交叉偶联反应。对于许多底物,获得的转化率和选择性结果极好,与活性更高甚至均相的催化剂所提供的结果相似。使用2--3,4,5-三甲氧基苯甲醛作为偶合伙伴,该方法同样有效,并获得了高收率的产品。此外,已表明其可用于合成三联苯四联苯。通过简单的过滤从反应中定量回收催化剂,并重复使用多个循环,而活性没有明显损失。
  • CATALYST FOR ASYMMETRIC HYDROGENATION AND METHOD FOR MANUFACTURING OPTICALLY ACTIVE CARBONYL COMPOUND USING THE SAME
    申请人:YAMADA Shinya
    公开号:US20120136176A1
    公开(公告)日:2012-05-31
    The present invention provides a catalyst used for manufacturing an optically active carbonyl compound by selective asymmetric hydrogenation of an α,β-unsaturated carbonyl compound, which is insoluble in a reaction mixture, and a method for manufacturing the corresponding optically active carbonyl compound. Particularly, the invention provides a catalyst for obtaining an optically active citronellal useful as a flavor or fragrance, by selective asymmetric hydrogenation of citral, geranial or neral. The invention relates to a catalyst for asymmetric hydrogenation of an α,β-unsaturated carbonyl compound, which comprises: a powder of at least one metal selected from metals belonging to Group 8 to Group 10 of the Periodic Table, or a metal-supported substance in which the at least one metal is supported on a support; an optically active peptide compound; and an acid, and also relates to a method for manufacturing an optically active carbonyl compound using the same.
    本发明提供了一种用于通过选择性不对称加氢α,β-不饱和羰基化合物制备光学活性羰基化合物的催化剂,该催化剂在反应混合物中不溶解,并提供了制备相应光学活性羰基化合物的方法。特别地,该发明提供了一种催化剂,通过选择性不对称加氢柠檬醛、香叶醛或柠檬醛制备出用作香料或芳香剂的光学活性香茅醛。该发明涉及一种用于不对称加氢α,β-不饱和羰基化合物的催化剂,包括:来自周期表第8至第10族属中至少一种属的粉末,或者至少一种属负载物质,其中至少一种属负载在一种载体上;一种光学活性肽化合物;和一种酸,还涉及使用该催化剂制备光学活性羰基化合物的方法。
  • Sulfur(VI) fluoride compounds and methods for the preparation thereof
    申请人:The Scripps Research Institute
    公开号:US10117840B2
    公开(公告)日:2018-11-06
    This application describes a compound represented by Formula (I): (I) wherein: Y is a biologically active organic core group comprising one or more of an aryl group, a heteroaryl aryl group, a nonaromatic hydrocarbyl group, and a nonaromatic heterocyclic group, to which Z is covalently bonded; n is 1, 2, 3, 4 or 5; m is 1 or 2; Z is O, NR, or N; X1 is a covalent bond or —CH2CH2—, X2 is O or NR; and R comprises H or a substituted or unsubstituted group selected from an aryl group, a heteroaryl aryl group, a nonaromatic hydrocarbyl group, and a nonaromatic heterocyclic group. Methods of preparing the compounds, methods of using the compounds, and pharmaceutical compositions comprising the compounds are described as well.
    该应用描述了由式(I)表示的化合物:(I)其中:Y是一个生物活性有机核心基团,包括芳基、杂芳基、非芳香烃基和非芳香杂环基中的一个或多个,其中Z与之以共价键结合;n为1、2、3、4或5;m为1或2;Z为O、NR或N;X1为共价键或—CH2CH2—,X2为O或NR;R包括H或从芳基、杂芳基、非芳香烃基和非芳香杂环基中选择的取代或未取代基团。还描述了制备这些化合物的方法、使用这些化合物的方法以及包含这些化合物的药物组合物。
  • CATALYST FOR ASYMMETRIC HYDROGENATION
    申请人:MAEDA Hironori
    公开号:US20100324338A1
    公开(公告)日:2010-12-23
    This invention aims at providing a catalyst for producing an optically active aldehyde or an optically active ketone, which is an optically active carbonyl compound, by carrying out selective asymmetric hydrogenation of an α,β-unsaturated carbonyl compound, particularly a catalyst which is insoluble in a reaction mixture for obtaining optically active citronellal which is useful as a flavor or fragrance, by carrying out selective asymmetric hydrogenation of citral, geranial or neral; and a method for producing a corresponding optically active carbonyl compound. The invention relates to a catalyst for asymmetric hydrogenation of an α,β-unsaturated carbonyl compound, which comprises a powder of at least one metal selected from metals belonging to Group 8 to Group 10 of the Periodic Table, or a metal-supported substance in which at least one metal selected from metals belonging to Group 8 to Group 10 of the Periodic Table is supported on a support, an optically active cyclic nitrogen-containing compound and an acid.
    这项发明旨在通过对α,β-不饱和羰基化合物进行选择性不对称加氢,特别是通过对柠檬醛、香叶醛或柠檬醛进行选择性不对称加氢,从而提供用作香料或香精的有用的光学活性香茅醛的催化剂,该香茅醛是一种光学活性羰基化合物;以及生产相应的光学活性羰基化合物的方法。该发明涉及一种用于不对称加氢α,β-不饱和羰基化合物的催化剂,其包括来自周期表第8至第10族属中至少一种属的粉末,或者至少一种来自周期表第8至第10族属的属负载物质,该属负载在一种支撑物上,还包括光学活性的含氮环化合物和酸。
  • METHOD FOR MANUFACTURING OPTICALLY ACTIVE MENTHOL
    申请人:Tsuda Toshiro
    公开号:US20130253228A1
    公开(公告)日:2013-09-26
    An object of the present invention is to provide a method for manufacturing an optically active menthol having fewer steps, which generates less environmentally polluting waste because a catalytic reaction is involved in all of the steps, and is capable of saving a production cost. The present invention relates to a method for manufacturing an optically active menthol, including the following steps: A-1) asymmetrically hydrogenating at least one of geranial and neral to thereby obtain an optically active citronellal, B-1) conducting a ring-closure reaction of the optically active citronellal in the presence of an acid catalyst to thereby obtain an optically active isopulegol, and C-1) hydrogenating the optically active isopulegol to thereby obtain an optically active menthol.
    本发明的目的是提供一种制造具有较少步骤的光学活性薄荷醇的方法,因为所有步骤都涉及催化反应,所以产生的环境污染废物较少,并且能够节省生产成本。本发明涉及一种制造光学活性薄荷醇的方法,包括以下步骤:A-1)不对称地氢化至少一种香叶醛和柠檬醛以获得光学活性柠檬醛,B-1)在酸催化剂存在下对光学活性柠檬醛进行环闭合反应,从而获得光学活性异薄荷醇,以及C-1)对光学活性异薄荷醇进行氢化以获得光学活性薄荷醇。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫