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1-苯氧基-4-(4-苯氧基苯基)苯 | 2519-16-6

中文名称
1-苯氧基-4-(4-苯氧基苯基)苯
中文别名
——
英文名称
4,4'-diphenoxybiphenyl
英文别名
4,4'-diphenoxy-1,1'-biphenyl;1-phenoxy-4-(4-phenoxyphenyl)benzene
1-苯氧基-4-(4-苯氧基苯基)苯化学式
CAS
2519-16-6
化学式
C24H18O2
mdl
——
分子量
338.406
InChiKey
RGCAQUUSBHVLJD-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:
    151 °C
  • 沸点:
    471.9±38.0 °C(Predicted)
  • 密度:
    1.143±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.6
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • SUBSTITUTED OR UNSUBSTITUTED ALLYL GROUP-CONTAINING MALEIMIDE COMPOUND, PRODUCTION METHOD THEREFOR, AND COMPOSITION AND CURED PRODUCT USING SAID COMPOUND
    申请人:DIC CORPORATION
    公开号:US20200325101A1
    公开(公告)日:2020-10-15
    Bismaleimides (BMI) exhibit excellent heat resistance (high Tg and high resistance to thermal decomposition) compared to epoxy resins and phenolic resins, and therefore, in recent years, more attention is paid to bismaleimides as a resin material for the next-generation devices represented by SiC power semiconductors, in addition to the investigation on the use of bismaleimides for electronic material applications. As such, conventional BMI's are known as highly heat-resistant resins; however, there is a demand for a resin having higher heat resistance for advanced material applications and the like. Thus, an object of the invention is to provide a novel maleimide compound having superior heat resistance. Disclosed is a substituted or unsubstituted allyl group-containing maleimide compound having a structure with three or more benzene rings, having one or more groups each having a substituted or unsubstituted allyl group, and having one or more maleimide groups.
    亚苯基马来酰亚胺化合物,具有三个或更多苯环的结构,含有一个或多个取代或未取代的烯丙基团,以及一个或多个马来酰亚胺基团,具有卓越的耐热性。
  • Miyaura Borylation and One-Pot Two-Step Homocoupling of Aryl Chlorides and Bromides under Solvent-Free Conditions
    作者:Pavel B. Dzhevakov、Maxim A. Topchiy、Daria A. Zharkova、Oleg S. Morozov、Andrey F. Asachenko、Mikhail S. Nechaev
    DOI:10.1002/adsc.201500844
    日期:2016.3.17
    borylation and the one‐pot, two‐step homocoupling of aryl halides are reported for the first time. Bis(dibenzylideneacetone)palladium(0) [Pd(dba)2] is an optimal source of palladium for Miyaura borylation, while for one‐pot two‐step homocoupling palladium(II) acetate [Pd(OAc)2] gives highest yields. Aryl bromides are coupled most efficiently using the DPEphos ligand. Chlorides are coupled using XPhos. The
    首次报道了宫浦硼化反应的无溶剂方案和芳基卤化物的一锅,两步均偶联。双(二亚苄基丙酮)钯(0)​​[Pd(dba)2 ]是用于宫浦硼酸化的最佳钯来源,而对于一锅两步均偶联的乙酸钯(II)[Pd(OAc)2 ]则可提供最高的收率。使用DPEphos配体可以最有效地偶联芳基溴化物。氯化物使用XPhos偶联。所开发的协议功能强大,用途广泛且易于大规模复制。
  • METHOD FOR MANUFACTURING CONJUGATED AROMATIC COMPOUND
    申请人:Oda Seiji
    公开号:US20110275859A1
    公开(公告)日:2011-11-10
    A method for manufacturing a conjugated aromatic compound comprising reacting an aromatic compound (A) wherein one or two leaving groups selected from the group consisting of an iodine atom, a bromine atom and a chlorine atom are bonded to an aromatic ring and the aromatic compound (A) does not have (c1) a group represented by the following formula (10): wherein A 1 represents a C1-C20 alkoxy group etc.; (g1) a C1-C20 alkyl group which may be substituted with a fluorine atom etc.; and (h1) a C2-C20 acyl group which may be substituted with a fluorine atom etc., at the neighboring carbon atom to the carbon atom to which the leaving group is bonded, with an aromatic compound (A) having the same structure as that of the above-mentioned aromatic compound (A) or an aromatic compound (B) wherein the aromatic compound (B) is structurally different from the above-mentioned aromatic compound (A), one or two leaving groups selected from the group consisting of an iodine atom, a bromine atom and a chlorine atom are bonded to an aromatic ring and the aromatic compound (B) does not have the above-mentioned (c1), (g1) and (h1) at the neighboring carbon atom to the carbon atom to which the leaving group is bonded, in the presence of (i) a nickel compound, (ii) a metal reducing agent, (iii) at least one ligand (L1) selected from the group consisting of a 2,2′-bipyridine compound having at least one electron-withdrawing group and having no substituent at 3-, 6-, 3′- and 6′-positions, and a 1,10-phenanthroline compound having at least one electron-withdrawing group and having no substituent at 2- and 9-positions, and (iv) at least one ligand (L2) selected from the group consisting of a 2,2′-bipyridine compound having at least one electron-releasing group and having no substituent at 3-, 6-, 3′- and 6′-positions, and a 1,10-phenanthroline compound having at least one electron-releasing group and having no substituent at 2- and 9-positions.
    一种制备共轭芳香化合物的方法,包括将含有一个或两个离去基团的芳香化合物(A)与含有相同结构的上述芳香化合物(A)或结构不同的芳香化合物(B)反应,其中这些离去基团选自碘原子、溴原子和氯原子,与芳香环结合,而芳香化合物(A)没有以下式(10)所代表的基团:其中A1代表C1-C20烷氧基等;(g1)代表C1-C20烷基基团,可能被氟原子等取代;以及(h1)代表C2-C20酰基基团,可能被氟原子等取代,与离去基团结合的碳原子的相邻碳原子处没有上述(c1)、(g1)和(h1),在(i)镍化合物、(ii)金属还原剂、(iii)从2,2′-联吡啶化合物和1,10-邻菲啰啉化合物中选择的至少一种配体(L1),具有至少一个吸电子基团且在3-、6-、3′-和6′-位置没有取代基,以及(iv)从2,2′-联吡啶化合物和1,10-邻菲啰啉化合物中选择的至少一种配体(L2),具有至少一个释电子基团且在3-、6-、3′-和6′-位置没有取代基团的情况下,在上述离去基团结合的碳原子的相邻碳原子处进行反应。
  • The palladium(II)/carbon monoxide-mediated biaryl formation from aryltellurium trihalides
    作者:Hidetaka Takahashi、Kouichi Ohe、Sakae Uemura、Nobuyuki Sugita
    DOI:10.1016/0022-328x(88)80378-4
    日期:1988.8
    4-MeOC6H4, 4-BuOC6H4, 4-PhOC6H4, 2-naphthyl; X = Cl, Br) with a palladium(II) salt in acetonitrile at 25°C affords, in good yields (29–78%), the corresponding biaryls (ArAr) either in the atmosphere or under 1 atm CO. The presence of CO accelerates this aromatic coupling significantly to produce some active palladium carbonyl species, the formation of which was confirmed by IR spectroscopy of Li2PdCl4 in
    aryltellurium三卤化物(抽纱的治疗3:Ar为PH,4- BRC 6 ħ 4,4-MEC 6 ħ 4,4-MeOC 6 H ^ 4,4-BuOC 6 ħ 4,4-PhOC 6 ħ 4,2-萘基; X = Cl,Br)和钯(II)盐在25°C的乙腈溶液中,可在大气中或低于1个大气压的条件下,以良好的收率(29-78%)提供相应的联芳基(ArAr)。的CO大大加速了这种芳族偶联,从而产生了一些活性的羰基钯物种,其形成已通过Li 2 PdCl 4的红外光谱证实在乙腈溶液中于一氧化碳; (Pd = C = O)物种的ν(C = O)分别在2140和1908 cm -1处显示出强烈的尖锐吸收和较弱的尖锐吸收。反应后用碱处理对于产生联芳基是必不可少的。
  • Ligand- and Counterion-Assisted Phenol <i>O</i>-Arylation with TMP-Iodonium(III) Acetates
    作者:Kotaro Kikushima、Naoki Miyamoto、Kazuma Watanabe、Daichi Koseki、Yasuyuki Kita、Toshifumi Dohi
    DOI:10.1021/acs.orglett.2c00294
    日期:2022.3.18
    High reactivity of trimethoxyphenyl (TMP)-iodonium(III) acetate for phenol O-arylation was achieved. It was first determined that the TMP ligand and acetate anion cooperatively enhance the electrophilic reactivity toward phenol oxygen atoms. The proposed method provides access to various diaryl ethers in significantly higher yields than the previously reported techniques. Various functional groups
    实现了三甲氧基苯基 (TMP)-碘鎓 (III) 乙酸酯对苯酚O-芳基化的高反应性。首先确定 TMP 配体和乙酸根阴离子协同增强对苯酚氧原子的亲电反应性。与先前报道的技术相比,所提出的方法以显着更高的产率提供了获得各种二芳基醚的途径。在O-芳基化过程中可以耐受各种官能团,包括脂肪醇、硼酸酯和空间位阻基团,验证了这种配体和抗衡离子辅助策略的适用性。
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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)-(-)-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)-(+)-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)-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 (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 (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 (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-[[[[[[((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 (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 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐