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Dimethyl 5-[2-[15,24-bis[2-[3,5-bis(methoxycarbonyl)phenyl]ethynyl]-9,9,18,18,27,27-hexakis[2-(2-methoxyethoxy)ethyl]-6-heptacyclo[18.7.0.02,10.03,8.011,19.012,17.021,26]heptacosa-1,3(8),4,6,10,12(17),13,15,19,21(26),22,24-dodecaenyl]ethynyl]benzene-1,3-dicarboxylate | 1353566-90-1

中文名称
——
中文别名
——
英文名称
Dimethyl 5-[2-[15,24-bis[2-[3,5-bis(methoxycarbonyl)phenyl]ethynyl]-9,9,18,18,27,27-hexakis[2-(2-methoxyethoxy)ethyl]-6-heptacyclo[18.7.0.02,10.03,8.011,19.012,17.021,26]heptacosa-1,3(8),4,6,10,12(17),13,15,19,21(26),22,24-dodecaenyl]ethynyl]benzene-1,3-dicarboxylate
英文别名
dimethyl 5-[2-[15,24-bis[2-[3,5-bis(methoxycarbonyl)phenyl]ethynyl]-9,9,18,18,27,27-hexakis[2-(2-methoxyethoxy)ethyl]-6-heptacyclo[18.7.0.02,10.03,8.011,19.012,17.021,26]heptacosa-1,3(8),4,6,10,12(17),13,15,19,21(26),22,24-dodecaenyl]ethynyl]benzene-1,3-dicarboxylate
Dimethyl 5-[2-[15,24-bis[2-[3,5-bis(methoxycarbonyl)phenyl]ethynyl]-9,9,18,18,27,27-hexakis[2-(2-methoxyethoxy)ethyl]-6-heptacyclo[18.7.0.02,10.03,8.011,19.012,17.021,26]heptacosa-1,3(8),4,6,10,12(17),13,15,19,21(26),22,24-dodecaenyl]ethynyl]benzene-1,3-dicarboxylate化学式
CAS
1353566-90-1
化学式
C93H102O24
mdl
——
分子量
1603.82
InChiKey
PYIWVCSSAUJOOF-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):
    11.8
  • 重原子数:
    117
  • 可旋转键数:
    54
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    269
  • 氢给体数:
    0
  • 氢受体数:
    24

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:
    描述:
    Dimethyl 5-[2-[15,24-bis[2-[3,5-bis(methoxycarbonyl)phenyl]ethynyl]-9,9,18,18,27,27-hexakis[2-(2-methoxyethoxy)ethyl]-6-heptacyclo[18.7.0.02,10.03,8.011,19.012,17.021,26]heptacosa-1,3(8),4,6,10,12(17),13,15,19,21(26),22,24-dodecaenyl]ethynyl]benzene-1,3-dicarboxylate 、 potassium hydroxide 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 24.0h, 以75%的产率得到5-[2-[15,24-Bis[2-(3,5-dicarboxyphenyl)ethynyl]-9,9,18,18,27,27-hexakis[2-(2-methoxyethoxy)ethyl]-6-heptacyclo[18.7.0.02,10.03,8.011,19.012,17.021,26]heptacosa-1,3(8),4,6,10,12(17),13,15,19,21(26),22,24-dodecaenyl]ethynyl]benzene-1,3-dicarboxylic acid
    参考文献:
    名称:
    Water-soluble anionic fluorophores from truxene
    摘要:
    Two new water-soluble fluorophores are synthesized from truxene and ester-substituted aryl acetylenes. The truxene core is decorated by 2-(2'-methoxy)ethoxyethyl groups to enhance the hydrophilicity of these fluorophores as well as to prevent the aggregation by pi-stacking in aqueous media. The conjugated structures are assembled by iodination of the truxene core and subsequent Sonogashira coupling with aryl acetylenes. Upon the hydrolysis of the ester groups, water-soluble fluorophores are obtained in good to excellent yield (30-71% for 3 steps). A photophysical investigation reveals that these compounds exhibit strong fluorescence signals (quantum yield 46-63%) with maximum emission wavelength around 390-400 nm in aqueous phosphate buffer. Preliminary screening on sensing application shows that their fluorescent signals can be selectively quenched by porphyrin-containing metalloproteins. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2011.10.009
  • 作为产物:
    描述:
    2,7,12-triiodo-5,5',10,10',15,15'-hexa-2-(2-methoxyethoxy)ethyltruxene 、 5-乙炔基间苯二甲酸二甲酯 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 甲苯 为溶剂, 反应 24.0h, 以43%的产率得到Dimethyl 5-[2-[15,24-bis[2-[3,5-bis(methoxycarbonyl)phenyl]ethynyl]-9,9,18,18,27,27-hexakis[2-(2-methoxyethoxy)ethyl]-6-heptacyclo[18.7.0.02,10.03,8.011,19.012,17.021,26]heptacosa-1,3(8),4,6,10,12(17),13,15,19,21(26),22,24-dodecaenyl]ethynyl]benzene-1,3-dicarboxylate
    参考文献:
    名称:
    Water-soluble anionic fluorophores from truxene
    摘要:
    Two new water-soluble fluorophores are synthesized from truxene and ester-substituted aryl acetylenes. The truxene core is decorated by 2-(2'-methoxy)ethoxyethyl groups to enhance the hydrophilicity of these fluorophores as well as to prevent the aggregation by pi-stacking in aqueous media. The conjugated structures are assembled by iodination of the truxene core and subsequent Sonogashira coupling with aryl acetylenes. Upon the hydrolysis of the ester groups, water-soluble fluorophores are obtained in good to excellent yield (30-71% for 3 steps). A photophysical investigation reveals that these compounds exhibit strong fluorescence signals (quantum yield 46-63%) with maximum emission wavelength around 390-400 nm in aqueous phosphate buffer. Preliminary screening on sensing application shows that their fluorescent signals can be selectively quenched by porphyrin-containing metalloproteins. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2011.10.009
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文献信息

  • Water-soluble anionic fluorophores from truxene
    作者:Nopporn Earmrattana、Mongkol Sukwattanasinitt、Paitoon Rashatasakhon
    DOI:10.1016/j.dyepig.2011.10.009
    日期:2012.4
    Two new water-soluble fluorophores are synthesized from truxene and ester-substituted aryl acetylenes. The truxene core is decorated by 2-(2'-methoxy)ethoxyethyl groups to enhance the hydrophilicity of these fluorophores as well as to prevent the aggregation by pi-stacking in aqueous media. The conjugated structures are assembled by iodination of the truxene core and subsequent Sonogashira coupling with aryl acetylenes. Upon the hydrolysis of the ester groups, water-soluble fluorophores are obtained in good to excellent yield (30-71% for 3 steps). A photophysical investigation reveals that these compounds exhibit strong fluorescence signals (quantum yield 46-63%) with maximum emission wavelength around 390-400 nm in aqueous phosphate buffer. Preliminary screening on sensing application shows that their fluorescent signals can be selectively quenched by porphyrin-containing metalloproteins. (C) 2011 Elsevier Ltd. All rights reserved.
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