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1-(4-(phenanthren-9-yl)phenyl)ethanone | 756484-28-3

中文名称
——
中文别名
——
英文名称
1-(4-(phenanthren-9-yl)phenyl)ethanone
英文别名
1-(4-(Phenanthren-9-yl)phenyl)ethan-1-one;1-(4-phenanthren-9-ylphenyl)ethanone
1-(4-(phenanthren-9-yl)phenyl)ethanone化学式
CAS
756484-28-3
化学式
C22H16O
mdl
——
分子量
296.368
InChiKey
WLSLINRRTLBIQB-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:
    469.8±14.0 °C(Predicted)
  • 密度:
    1.164±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.7
  • 重原子数:
    23
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    1-(4-(phenanthren-9-yl)phenyl)ethanone 、 methyl-2-(((diphenylmethylene)amino)oxy)-2-oxoacetate 在 9-噻吨酮 作用下, 以 乙酸乙酯 为溶剂, 反应 12.0h, 以22%的产率得到Methyl-10-(4-acetylphenyl)-10-((diphenylmethylene)amino)-9,10-dihydrophenanthrene-9-carboxylate
    参考文献:
    名称:
    烯烃和(杂)芳烃光化学单步合成 β-氨基酸衍生物
    摘要:
    β-氨基酸经常被发现是许多生物活性分子、药物和天然产物中的重要成分。特别是,由于它们提高了代谢稳定性,它们被广泛用于构建生物活性肽和肽模拟物。尽管建立了许多用于制备 β-氨基酸衍生物的方法,但这些方法中的大多数都需要金属介导的预功能化底物的多步操作。在这里,我们公开了一种无金属、能量转移的高区域选择性分子间氨基羧化反应,用于将胺和酯官能团单步安装到烯烃或(杂)芳烃中。开发了一种双功能肟草酸酯以同时产生以 C 为中心的酯和以 N 为中心的亚氨基自由基。
    DOI:
    10.1038/s41557-022-01008-w
  • 作为产物:
    描述:
    2-氨基联苯 在 tetrafluoroboric acid 、 eosin 、 sodium nitrite 作用下, 以 乙腈 为溶剂, 反应 12.5h, 生成 1-(4-(phenanthren-9-yl)phenyl)ethanone
    参考文献:
    名称:
    曙红Y催化可见光诱导的[4 + 2]联芳重氮盐与炔烃苯并菲的菲的合成
    摘要:
    开发了一种无金属,可见光诱导的联炔重氮盐与炔烃的[4 + 2]苯环。以曙红Y为光氧化还原催化剂,通过级联自由基加成和环化顺序获得了多种9-取代或9,10-二取代的菲。
    DOI:
    10.1002/adsc.201200569
点击查看最新优质反应信息

文献信息

  • Invisible Chelating Effect Exhibited between Carbodicarbene and Phosphine through π–π Interaction and Implication in the Cross-Coupling Reaction
    作者:Wei-Chih Shih、Yun-Ting Chiang、Qing Wang、Ming-Chun Wu、Glenn P. A. Yap、Lili Zhao、Tiow-Gan Ong
    DOI:10.1021/acs.organomet.7b00692
    日期:2017.11.13
    Palladium complexes supported with the mixed ligands carbodicarbene (CDC) and different phosphine ligands (PPh3, PTol3, and PCy3) were prepared, and their molecular structures were characterized. Examination of the structures of 2-PPh3 and 2-PTol3 with cis configuration discloses the existence of an unexpected π–π interaction between one phenyl group of the phosphine and the benzimidazole ring of a
    制备了由混合配体碳二碳烯(CDC)和不同的膦配体(PPh 3,PTol 3和PCy 3)负载的配合物,并对其分子结构进行了表征。对具有顺式构型的2-PPh 3和2-PTol 3的结构的研究揭示了膦的一个苯基与CDC的苯并咪唑环之间存在意想不到的π-π相互作用。配合物2-PPh 3是一种活性的铃木-宫浦催化剂,具有广泛的底物,包含各种官能团和空间要求。与吸电子芳基相反,通过在需氧条件下添加催化量的DMSO,可以提高富电子底物的产品收率。溶液NMR和结构分析表明,CDC和膦配体之间的分子内π-π相互作用对反应的活性具有积极影响,这进一步得到了量子化学计算的支持。
  • Synthesis of Functionalized Phenanthrenes via Regioselective Oxidative Radical Cyclization
    作者:Kamalkishore Pati、Christopher Michas、David Allenger、Ilya Piskun、Peter S. Coutros、Gabriel dos Passos Gomes、Igor V. Alabugin
    DOI:10.1021/acs.joc.5b01014
    日期:2015.12.4
    preparation of fully conjugated molecules. In this work, we report an oxidatively terminated Bu3Sn-mediated cyclization of an alkyne where AIBN, the commonly used initiator, takes on a new function as an oxidative agent. Sn-mediated radical transformation of biphenyl aryl acetylenes into functionalized phenanthrenyl stannanes can be initiated via two potentially equilibrating vinyl radicals, one of which can
    大多数Sn介导的环化反应都是还原性的,因此无法得到完全结合的产物。这是在Sn介导的自由基级联用于制备完全共轭分子的应用中的限制。在这项工作中,我们报告了氧化终止的Bu 3Sn介导的炔烃环化反应,其中常用的引发剂AIBN作为氧化剂起新的作用。可以通过两个可能平衡的乙烯基自由基引发联苯芳基乙炔的Sn介导的自由基转化为官能化的,其中一个可以被联苯部分的快速6内环合捕获,收率好至极好。Sn取代的有效制备为大型聚芳烃的构建提供了方便的构建基块。
  • Aromatic heterocyclic derivative, material for organic electroluminescent element, and organic electroluminescent element
    申请人:IDEMITSU KOSAN CO., LTD.
    公开号:US10199580B2
    公开(公告)日:2019-02-05
    An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y1 is an oxygen atom, a sulfur atom or the like, and one of X11 to X18 is a carbon atom bonded to L1 by a single bond and the rest of X11 to X18 are a nitrogen atom or CR13
    一种有机电致发光器件依次包括阳极、发光层、电子传输区和阴极,其中电子传输区包含由下式(1)表示的芳香杂环衍生物。式(1)中,X1 至 X3 为氮原子或 CR1,A 由下式(2)表示。在式 (2) 中,L1 是单键或连接基团,HAr 用下式 (3) 表示。在式 (3) 中,Y1 是氧原子、原子或类似物,X11 至 X18 中的一个是通过单键与 L1 结合的碳原子,X11 至 X18 中的其余部分是氮原子或 CR13。
  • AROMATIC HETEROCYCLIC DERIVATIVE, MATERIAL FOR ORGANIC ELECTROLUMINESCENCE ELEMENT, AND ORGANIC ELECTROLUMINESCENCE ELEMENT
    申请人:Idemitsu Kosan Co., Ltd.
    公开号:US20140073784A1
    公开(公告)日:2014-03-13
    An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X 1 to X 3 are a nitrogen atom or CR 1 , and A is represented by a formula (2) below. In the formula (2), L 1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y 1 is an oxygen atom, a sulfur atom or the like, and one of X 11 to X 18 is a carbon atom bonded to L 1 by a single bond and the rest of X 11 to X 18 are a nitrogen atom or CR 13 .
  • AROMATIC HETEROCYCLIC DERIVATIVE, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, AND ORGANIC ELECTROLUMINESCENT ELEMENT
    申请人:IDEMITSU KOSAN CO., LTD.
    公开号:US20160111655A1
    公开(公告)日:2016-04-21
    An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X 1 to X 3 are a nitrogen atom or CR 1 , and A is represented by a formula (2) below. In the formula (2), L 1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y 1 is an oxygen atom, a sulfur atom or the like, and one of X 11 to X 18 is a carbon atom bonded to L 1 by a single bond and the rest of X 11 to X 18 are a nitrogen atom or CR 13 .
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