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diethyl 2,5-di(thiophen-2-yl)thiophene-3,4-dicarboxylate | 1041440-98-5

中文名称
——
中文别名
——
英文名称
diethyl 2,5-di(thiophen-2-yl)thiophene-3,4-dicarboxylate
英文别名
Diethyl 2,5-dithiophen-2-ylthiophene-3,4-dicarboxylate;diethyl 2,5-dithiophen-2-ylthiophene-3,4-dicarboxylate
diethyl 2,5-di(thiophen-2-yl)thiophene-3,4-dicarboxylate化学式
CAS
1041440-98-5
化学式
C18H16O4S3
mdl
——
分子量
392.521
InChiKey
YWGUMQPBILCZQP-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:
    522.5±50.0 °C(Predicted)
  • 密度:
    1.320±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.8
  • 重原子数:
    25
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    137
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    diethyl 2,5-di(thiophen-2-yl)thiophene-3,4-dicarboxylate 作用下, 以 甲醇 为溶剂, 生成 TTT-Lum
    参考文献:
    名称:
    Synthesis and properties of a novel redox driven chemiluminescent material built on a terthienyl system
    摘要:
    A novel redox driven chemiluminescent material built on a terthienyl system, namely 5,7-di-ethylenedioxythiophen-2-yl-2,3-dihydro-thieno[3,4-d]pyridazine-1,4-dione (ETE-Lum), which is soluble in both organic media and basic aqueous solution was synthesized and characterized. Furthermore, its polymer, PETE-Lum, which is one of the most rare examples of chemiluminescent polymeric materials bearing a pyridazine unit, was obtained successfully by electrochemical means. Both of the materials give chemiluminescence either by treatment with oxidants (H2O2 and/or KMnO4) or by the application of a potential pulse. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.05.019
  • 作为产物:
    描述:
    二乙基噻吩-2,6-二溴-3,4-二羧酸酯2-(trimethylstannyl)thiophene 在 bis-triphenylphosphine-palladium(II) chloride 作用下, 以 甲苯 为溶剂, 以40%的产率得到diethyl 2,5-di(thiophen-2-yl)thiophene-3,4-dicarboxylate
    参考文献:
    名称:
    A glow in the dark: synthesis and electropolymerization of a novel chemiluminescent terthienyl system
    摘要:
    本文介绍了一种基于噻吩基体系的独特(电)化学发光单体及其相应聚合物的合成和表征,这种聚合物是首例带有哒嗪附属物的电活性化学发光聚合物。
    DOI:
    10.1039/b814258k
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文献信息

  • Synthesis and properties of a novel redox driven chemiluminescent material built on a terthienyl system
    作者:Nurdan Atılgan、Fatih Algı、Ahmet M. Önal、Atilla Cihaner
    DOI:10.1016/j.tet.2009.05.019
    日期:2009.7
    A novel redox driven chemiluminescent material built on a terthienyl system, namely 5,7-di-ethylenedioxythiophen-2-yl-2,3-dihydro-thieno[3,4-d]pyridazine-1,4-dione (ETE-Lum), which is soluble in both organic media and basic aqueous solution was synthesized and characterized. Furthermore, its polymer, PETE-Lum, which is one of the most rare examples of chemiluminescent polymeric materials bearing a pyridazine unit, was obtained successfully by electrochemical means. Both of the materials give chemiluminescence either by treatment with oxidants (H2O2 and/or KMnO4) or by the application of a potential pulse. (C) 2009 Elsevier Ltd. All rights reserved.
  • A glow in the dark: synthesis and electropolymerization of a novel chemiluminescent terthienyl system
    作者:Demet Asil、Atilla Cihaner、Ahmet M. Önal
    DOI:10.1039/b814258k
    日期:——
    The synthesis and characterization of a unique (electro)chemiluminescent monomer based on a terthienyl system, and its corresponding polymer which is the first example of an electro-active chemiluminescent polymer bearing a pyridazine appendage, are described.
    本文介绍了一种基于噻吩基体系的独特(电)化学发光单体及其相应聚合物的合成和表征,这种聚合物是首例带有哒嗪附属物的电活性化学发光聚合物。
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同类化合物

试剂2,2'-Thieno[3,2-b]thiophene-2,5-diylbis-3-thiophenecarboxylicacid 苯并[b]噻吩,3-(2-噻嗯基)- 甲基[2,3'-联噻吩]-5-羧酸甲酯 牛蒡子醇 B 十四氟-Alpha-六噻吩 三丁基(5''-己基-[2,2':5',2''-三联噻吩]-5-基)锡 α-四联噻吩 α-六噻吩 α-五联噻吩 α-七噻吩 α,ω-二己基四噻吩 5,5′-双(3-己基-2-噻吩基)-2,2′-联噻吩 α,ω-二己基六联噻吩 Α-八噻吩 alpha-三联噻吩甲醇 alpha-三联噻吩 [3,3-Bi噻吩]-2,2-二羧醛 [2,2’]-双噻吩-5,5‘-二甲醛 [2,2':5',2''-三联噻吩]-5,5''-二基双[三甲基硅烷] [2,2'-联噻吩]-5-甲醇,5'-(1-丙炔-1-基)- [2,2'-联噻吩]-5-甲酸甲酯 [2,2'-联噻吩]-5-乙酸,a-羟基-5'-(1-炔丙基)-(9CI) C-[2,2-二硫代苯-5-基甲基]胺 5’-己基-2,2’-联噻吩-5-硼酸频哪醇酯 5-辛基-1,3-二(噻吩-2-基)-4H-噻吩并[3,4-c]吡咯-4,6(5H)-二酮 5-苯基-2,2'-联噻吩 5-溴5'-辛基-2,2'-联噻吩 5-溴-5′-己基-2,2′-联噻吩 5-溴-5'-甲酰基-2,2':5'2'-三噻吩 5-溴-3,3'-二己基-2,2'-联噻吩 5-溴-3'-癸基-2,2':5',2''-三联噻吩 5-溴-2,2-双噻吩 5-溴-2,2'-联噻吩-5'-甲醛 5-氯-5'-苯基-2,2'-联噻吩 5-氯-2,2'-联噻吩 5-正辛基-2,2'-并噻吩 5-己基-5'-乙烯基-2,2'-联噻吩 5-己基-2,2-二噻吩 5-全氟己基-5'-溴-2,2'-二噻吩 5-全氟己基-2,2′-联噻吩 5-乙酰基-2,2-噻吩基 5-乙氧基-2,2'-联噻吩 5-丙酰基-2,2-二噻吩 5-{[[2,2'-联噻吩]-5-基}噻吩-2-腈 5-[5-(5-己基噻吩-2-基)噻吩-2-基]噻吩-2-羧酸 5-(羟甲基)-[2,2]-联噻吩 5-(噻吩-2-基)噻吩-2-甲腈 5-(5-甲酰基-3-己基噻吩-2-基)-4-己基噻吩-2-甲醛 5-(5-甲基噻吩-2-基)噻吩-2-甲醛 5-(5-噻吩-2-基噻吩-2-基)噻吩-2-羧酸 5-(5-乙炔基噻吩-2-基)噻吩-2-甲醛