1415934-97-2

Upstream product

• 517-22-6 2,4-dimethyl-3-ethyl-pyrrole 
• 1415935-04-4 3-chloro-8-ethyl-5,5-difluoro-7,9-dimethyl-10-phenyl-5H-5λ⁴,6λ⁴-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinine-2-carbaldehyde 
• 1415935-02-2 8-ethyl-5,5-difluoro-7,9-dimethyl-10-phenyl-3-(propylamino)-5H-5λ⁴,6λ⁴-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinine-2-carbaldehyde 
• 141-97-9 ethyl acetoacetate 
• 1355953-59-1 3-chloro-5,7-dimethyl-6-ethyl-8-phenyl-BODIPY 

Downstream Products

• 1415935-05-5 C₂₈H₃₁BF₂N₄O₂ 
• 1415935-06-6 C₂₉H₃₄BF₂N₅O₃ 

Relevant academic research and scientific papers

COMPOUND AND ORGANIC PHOTOELECTRONIC DEVICE AND IMAGE SENSOR

The present invention relates to a compound represented by chemical formula 1; an organic photoelectronic device comprising a first electrode and a second electrode which face each other and an active layer which is placed between the first electrode and the second electrode and includes the compound represented by chemical formula 1; and an image sensor comprising the organic photoelectronic device.COPYRIGHT KIPO 2016

Pyridone fused boron-dipyrromethenes: Synthesis and properties

In this paper a general procedure for the introduction of pyridone moiety was developed, using a Friedlaender reaction, for post-modification of ready-made BODIPY core, from which three pyridone-fused BODIPYs 1, 2 and 3 were generated. This method is complementary to the classical method for obtaining aromatic ring-fused BODIPYs, which begins with the condensation of the corresponding aromatic ring-fused pyrroles. These pyridone-fused BODIPYs are distinctive, possessing favorable photophysical characteristics with strong absorption, high bright orange fluorescence and easy reduction due to the electron-withdrawing effect of the fused pyridone moiety. More important, these BODIPYs bear reactive functions which are applicable in proteins labeling by bioorthogonal chemical reactions.