1165898-88-3

Upstream product

• 83-38-5 2,6-dichlorobenzaldehyde 
• 194796-34-4 (2,6-dichlorophenyl)dipyrrol-2-ylmethane 
• 84-58-2 2,3-dicyano-5,6-dichloro-p-benzoquinone 

Downstream Products

• 1269636-16-9 8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1269636-18-1 tert-butyl (8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacen-3-yl)acetate 
• 1269636-17-0 methyl (8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacen-3-yl)acetate 
• 1269636-19-2 8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1269636-20-5 3-phenacyl-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1269636-21-6 diethyl (8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacen-3-yl)malonate 
• 1269636-25-0 3-(4-methoxyphenylethenyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1269636-28-3 3-(2-naphthyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1269636-27-2 3-(4-N,N-dimethylaminophenylethenyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1341774-23-9 C₁₆H₉BCl₂F₂N₂O 

Relevant academic research and scientific papers

Synthesis and characterization of two novel red-shifted isothiocyanate BODIPYs and their application in protein conjugation

Fluorescent organic small molecules are very important tools for researchers in the fields of biochemistry and biotechnology, and boron-dipyrromethene (BODIPY) class of organic fluorophores gained much attention in recent years due to their remarkable pho

Synthesis and antiprotozoal activity of original porphyrin precursors and derivatives

Importance of heme in African trypanosomes, Leishmania sp. and Plasmodium sp. metabolisms justifies considering the potential of porphyrins and their precursors and derivatives as potential antiparasitic agents by interfering with heme metabolism. Consequ

Vicarious nucleophilic substitution of α-hydrogen of BODIPY and its extension to direct ethenylation

Direct, oxidizer-free substitution of the 3-hydrogen of BODIPY derivatives has been established through a vicarious nucleophilic substitution procedure. This methodology has been combined with a reversible Michael addition on nitrostyrenes to provide a novel, highly efficient entry to the valuable 3-styrylated BODIPY dyes.

α-/β-formylated boron-dipyrrin (BODIPY) dyes: Regioselective syntheses and photophysical properties

Formylation has been performed on pyrrole-unsubstituted dipyrromethanes 1 and boron-dipyrrin (BODIPY) dyes 4 based on a Vilsmeier-Haack reaction. It is highly regioselective and complementary and occurs exclusively at the α-and β-position, respectively, f

Facile synthesis of dicyanovinyl-di(meso-aryl)dipyrromethenes via a dipyrromethene-DDQ adduct

The dicyano-substituted vinyl dipyrromethene 4 and compound 5 are near-planar and were prepared from a simple meso-aryl dipyrromethane via the DDQ adduct 3; the unique structures of 3, 4 and 5 were confirmed by X-ray diffraction analysis.