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4-(2-(2-pyridinyl)ethenyl)phenyl acetate | 1149-57-1

中文名称
——
中文别名
——
英文名称
4-(2-(2-pyridinyl)ethenyl)phenyl acetate
英文别名
[4-(2-Pyridin-2-ylethenyl)phenyl] acetate
4-(2-(2-pyridinyl)ethenyl)phenyl acetate化学式
CAS
1149-57-1
化学式
C15H13NO2
mdl
——
分子量
239.274
InChiKey
KSTDUJJGAWWLFZ-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):
    2.9
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    39.2
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:9d9d45044443f839451d521d82f7215a
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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:
    参考文献:
    名称:
    Comparative Syntheses of Arylamine Monomer with Styrylpyridyl Photo-Crosslinker of Polyarylamine for OLED Hole-Injection Material
    摘要:
    A new arylamine monomer with photo-crosslinkable styrylpyridinyl moiety of conjugated polyarylamine for OLED hole injection material was synthesized through two synthetic routes, BOC-amine protection/deprotection and nitro group reduction methods. Both synthetic routes yielded practically pure amine product by standard aqueous workup and crystallization in 61% overall yield from pyridinylvinylphenol 2. Their reaction efficiencies were comparatively studied in views of practicality and reaction scale. Also, the synthetic conditions of key compound of photo-crosslinker, pyridinylvinylphenol 2 was reinvestigated and established for the reproducible and reliable preparation.
    DOI:
    10.1080/15421406.2010.499316
  • 作为产物:
    描述:
    4-乙酰氧基苯甲醛2-皮考基三苯基鏻氯化物 在 sodium hydride 作用下, 以 四氢呋喃 、 mineral oil 为溶剂, 反应 25.0h, 生成 4-(2-(2-pyridinyl)ethenyl)phenyl acetate
    参考文献:
    名称:
    硼烷催化的2-乙烯基取代的吡啶的化学选择性和对映选择性还原。
    摘要:
    在此,我们报道了首次实现了2-乙烯基取代吡啶的高度化学选择性和对映选择性的还原。该反应使用手性螺双环双硼烷作为催化剂,HBpin和酸性酰胺作为还原剂,通过包括1,4-氢硼化的级联过程进行,然后转移氢化二氢吡啶中间体。还原产物中保留的双键可通过简单转化将其转化为天然产物和其他有用的杂环化合物。
    DOI:
    10.1002/anie.202007352
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文献信息

  • Discovery of novel picolinamide-based derivatives as novel VEGFR-2 kinase inhibitors: synthesis,<i>in vitro</i>biological evaluation and molecular docking
    作者:Wuji Sun、Shubiao Fang、Hong Yan
    DOI:10.1039/c8md00057c
    日期:——
    Vascular endothelial growth factor receptor-2 (VEGFR-2) plays a crucial role in tumor angiogenesis, and inhibition of the VEGFR-2 signaling pathway has emerged as an attractive target for cancer therapy. In our effort, a novel series of picolinamide-based derivatives were designed and synthesized as potent and effective VEGFR-2 inhibitors. All the newly prepared compounds were evaluated in vitro for
    血管内皮生长因子受体2(VEGFR-2)在肿瘤血管生成中起着至关重要的作用,而对VEGFR-2信号通路的抑制已成为癌症治疗的诱人靶标。在我们的努力中,设计并合成了一系列新的基于吡啶酰胺的衍生物,它们是有效且有效的VEGFR-2抑制剂。在体外评估所有新制备的化合物对A549和HepG2细胞系的抗增殖活性。在新化合物中,8j和8l对A549和HepG2细胞系均表现出更好的活性。进行分子对接以研究与VEGFR-2(PDB代码:4ASD)的结合能力和结合方式。
  • 手性螺环双硼催化取代吡啶的不对称还原方法及其应用
    申请人:南开大学
    公开号:CN111499558B
    公开(公告)日:2022-10-18
    本发明提供了一种手性螺环双催化取代吡啶的不对称还原方法,包括制备手性螺环双催化剂:在充满氮气的手套箱中,向反应瓶中依次加入手性螺环双烯和二芳基化合物,向反应瓶中加入溶剂,搅拌,使其充分反应,得到手性螺环双催化剂;催化还原吡啶:向上述反应瓶中加入吡啶、二级胺、三正丁基苄基氯化铵频那醇硼烷和所述溶剂,在氮气氛围中搅拌至反应结束;减压蒸馏除去溶剂,柱层析分离得到手性哌啶。该方法反应条件温和、催化剂用量低、选择性好、官能团兼容性广,且不需借助过渡催化剂,解决了药物中间体合成中重属残留的问题。
  • Design, synthesis and biological evaluation of pyrimidine-based derivatives as VEGFR-2 tyrosine kinase inhibitors
    作者:Wuji Sun、Shengquan Hu、Shubiao Fang、Hong Yan
    DOI:10.1016/j.bioorg.2018.04.005
    日期:2018.8
    of the VEGFR-2 signaling pathway has already become an attractive approach for cancer therapy. In this study, a novel pyrimidine-based derivative 7j was designed as lead compound, and three series of potent VEGFR-2 inhibitors were synthesized and biologically evaluated against A549 and HepG2 cell lines. Compounds 7d, 9s and 13n exhibited superior inhibitory activities against A549 cell with IC50 ranged
    血管内皮生长因子受体2(VEGFR-2)在肿瘤血管生成中起着至关重要的作用,而抑制VEGFR-2信号通路已经成为癌症治疗的一种有吸引力的方法。在这项研究中,设计了一种新型的基于嘧啶的衍生物7j作为前导化合物,合成了三组有效的VEGFR-2抑制剂,并针对A549和HepG2细胞系进行了生物学评估。与Pazopanib(IC 50)相比,化合物7d,9s和13n对A549细胞的IC 50为9.19至13.17μM,对HepG2细胞的IC 50为11.94至18.21μM。 = 21.18和36.66μM)。另外,进行了分子对接研究以研究目标化合物与VEGFR-2之间的结合能力和结合方式。
  • Synthesis of New Conjugated Polymers as Hole Injection Layer and Performance of OLED Devices
    作者:Tae Wook Yoo、Chul Park、Nguyen Thi Mai、Dong Uk Kim、Lee Soon Park
    DOI:10.1080/15421406.2011.600145
    日期:2011.11.4
    The fluorene-based poly(dioctylfluorene-alt-biphenylamine)s with styrylpyridyl group were synthesized by using Pd-catalyzed polycondensation reaction. These hole injection/transport polymers showed very good solvent resistance after photo-crosslinking which could facilitate the subsequent spin coating of the emitting layer polymer solution. Moreover these polymers could be patterned by using distyrylpyridyl alkyl monomer (DSM) as crosslinking agents. The OLED devices with configuration of ITO/HIL/Alq(3):NPD/LiF/Al in which synthesized polymer was used as hole injection layer (HIL) were fabricated and their performance was compared with the commercially available PEDOT:PSS as HIL layer.
  • Synthesis and Photolithographic Property of Conjugated Polymers with Polyazomethine Structure
    作者:Sang Chul Ryu、Young Chul Jeong、Lee Soon Park
    DOI:10.1080/15421400903240803
    日期:2009.11.11
    Two different polyazomethine-type conjugated polymers, poly(phenoxiazine-3, 3'-dihydroxybensidine)(PZ-DHB) and poly(phenoxiazine-2,4-diamino-6-hydroxypyrimidine)(PZ-DHP) containing phenothiazine moiety and azomethine linkage in the main chain were synthesized by Schiff-base polycondensation reactions. The polymer poly(PZ-DHB) was converted to the photosensitive type, through Mitsunobu reaction by incorporation of a photocrosslinkable group, hydroxyhexyloxystyryl-2-pyridine(2-HHSP) into the polymer side chains. The photosensitive conjugated polymer, poly(PZ-DHB)-PS, exhibited both strong fluorescence emission at 555 nm and good patterning property in the standard photolithographic processes.
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