2-[N-ethyl-N-[4-[2-[2-(3,4-dibutyl)thiene-5-carbaldehyde]ethenyl]phenyl]amino]ethyl ethanoate | 1022089-91-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-[N-ethyl-N-[4-[2-[2-(3,4-dibutyl)thiene-5-carbaldehyde]ethenyl]phenyl]amino]ethyl ethanoate
• CAS: 1022089-91-3
• 化学式: C₂₇H₃₇NO₃S
• 分子量: 455.662
• InChiKey: AVXSGYJTFXPFDL-UHFFFAOYSA-N

反应信息

• 作为反应物：
  描述：

  2-[N-ethyl-N-[4-[2-[2-(3,4-dibutyl)thiene-5-carbaldehyde]ethenyl]phenyl]amino]ethyl ethanoate 在 sodium hydroxide 作用下， 以 乙醇 、 水 为溶剂， 生成 2-[2-[4-[N-ethyl-N-(2-hydroxyethyl)amino]phenyl]ethenyl]-3,4-dibutylthiene-5-carbaldehyde 、 2-[2-[4-[N-ethyl-N-(2-hydroxyethyl)amino]phenyl]ethenyl]-3,4-dibutylthiene-5-carbaldehyde
  参考文献：
  名称：

  Synthesis and nonlinear optical properties of linear and Λ-shaped pyranone-based chromophores

  摘要：

  New, pyranone-based chromophores were synthesized and their (nonlinear) optical properties were measured. The chromophores were prepared by first condensing an electron withdrawing group with pyranone, followed by reaction with an aldehyde-functionalized pi-conjugated bridged donor molecule. This approach enables one to easily incorporate the pyranone moiety and to prepare both linear and A-shaped chromophores. The (nonlinear) optical properties were measured using femtosecond hyper-Rayleigh scattering. These measurements demonstrated the advantages of this approach. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2008.02.009