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2-([1,1'-biphenyl]-2-yl)furan

中文名称
——
中文别名
——
英文名称
2-([1,1'-biphenyl]-2-yl)furan
英文别名
Furylbiphenyl;2-(2-phenylphenyl)furan
2-([1,1'-biphenyl]-2-yl)furan化学式
CAS
——
化学式
C16H12O
mdl
——
分子量
220.271
InChiKey
LOHDUIVZXSEASO-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):
    4.3
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    13.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    邻氨基苯甲酸2-([1,1'-biphenyl]-2-yl)furan亚硝酸异戊酯 作用下, 以 四氢呋喃 为溶剂, 反应 3.33h, 以16%的产率得到1-(4-biphenyl)oxabenzonorbornadiene
    参考文献:
    名称:
    Synthesis of C1-Substituted Oxabenzonorbornadienes
    摘要:
    Oxabenzonorbornadienes are valuable synthetic intermediates because they can serve as a general template with which to create highly substituted ring systems. However, to date, only very few C1-substituted oxabenzonorbornadienes have been reported. In this study, the synthesis of some C1-substituted oxabenzonorbornadienes was achieved by the Diels-Alder reaction between 2-substituted furans and benzyne. Moderate to good yields (16-80%) of the Diels-Alder reactions were observed. These C1-substituted oxabenzonorbornadienes will find applications as valuable synthetic intermediates and should be useful in studies of transition-metal-catalyzed reactions.
    DOI:
    10.1055/s-0032-1316686
  • 作为产物:
    描述:
    2-氨基联苯呋喃 在 iron oxide 、 亚硝酸特丁酯 作用下, 以 二甲基亚砜 为溶剂, 以75%的产率得到2-([1,1'-biphenyl]-2-yl)furan
    参考文献:
    名称:
    10.1002/chem.202401617
    摘要:
    A magnetically isolable iron oxide nanoparticles is introduced as an efficient heterogeneous photocatalyst for non‐directed C‒H arylation employing aryl diazonium salts as the aryl precursors. This first‐row transition metal‐based photocatalyst revealed versatile activities and is applicable to a wide range of substrates, demonstrating brilliant efficacy and superior recyclability. Detailed catalytic characterization describes the physical properties and redox behavior of the Fe‐catalyst. Adequate control experiments helped to establish the radical‐based mechanism for the C‒H arylation.
    DOI:
    10.1002/chem.202401617
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文献信息

  • Reaction of aryl triflates with heteroaryllithiums via aryne intermediates
    作者:Kelly Hardee Reuter、William J. Scott
    DOI:10.1021/jo00069a041
    日期:1993.8
    Unhindered aryl triflates react with a mixture of 1.5 equiv of LDA and 8-10 equiv of 2-lithiofuran at -78-degrees-C to form 2-arylfurans in 50-60% yield via the corresponding arynes. Regioisomeric ratios of products are similar to those observed for reactions of arynes with well-precedented nucleophiles, such as metal amides. Steric hindrance ortho to the triflate increases the cine to ipso ratio, but lowers overall yields due to enhanced nucleophilic attack at sulfur leading to formation of the corresponding phenol. Use of 2-lithiothiophene affords the analogous arylthiophene.
  • Synthesis and Spectrokinetic Studies of a New Family of Dimethyl [2<i>H</i>]-Chromenes: Dimethyl 6-Aryl-2,2Dimethyl-[2<i>H</i>]-Chromene-7,8-Dicarboxylates
    作者:Alain Maggiani、Arlette Tubul、Pierre Brun、André Samat
    DOI:10.1080/10587250008023846
    日期:2000.6.1
    The synthesis of a series of dimethyl 6-aryl-2,2-dimethyl-[2H]-chromene-7,8-dicarboxylates is described. The photochromic properties of this new family of dimethyl-[2H]-chromenes have been studied in solution, under continuous irradiation. The presence of the methoxycarbonyl groups was shown to stabilise the coloured forms. The fading rates are generally low in comparison with the standard "naked" chromenes in the same experimental conditions. This stabilisation depends on the solvent used. We could observe the presence of one permanent opened form. Moreover, it seems that the synthesised molecules have a strong resistance toward photodegradation.
  • PHOTOELECTRIC CONVERSION ELEMENT AND IMAGING APPARATUS
    申请人:SONY CORPORATION
    公开号:US20200274077A1
    公开(公告)日:2020-08-27
    A photoelectric conversion element of the present disclosure includes: a first electrode: a second electrode opposed to the first electrode; and an organic layer provided between the first electrode and the second electrode, and including an organic photoelectric conversion layer, and at least one layer included in the organic layer is formed including at least one kind of organic semiconductor material represented by a general expression (1).
  • [EN] WATER-SOLUBLE FILM-MADE PACKAGE WITH FLUORESCENT DYE IN THE FILM<br/>[FR] EMBALLAGE COMPOSE D'UNE PELLICULE SOLUBLE DANS L'EAU CONTENANT UN COLORANT FLUORESCENT
    申请人:UNILEVER NV
    公开号:WO2003026982A1
    公开(公告)日:2003-04-03
    A water-soluble single-use package for a detergent composition comprising a fluorescent dye of limited water solubility in the water-soluble body portion. Preferred detergent compositions are low water-content liquid detergent compositions. A process of preparing a water-soluble film containing a fluorescent dye is also disclosed.
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