1269636-16-9

Upstream product

• 1165898-88-3 5-(2,6-Dichlorophenyl)dipyrromethene 
• 83-38-5 2,6-dichlorobenzaldehyde 
• 194796-34-4 (2,6-dichlorophenyl)dipyrrol-2-ylmethane 
• 109-63-7 boron trifluoride diethyl etherate 

Downstream Products

• 1269636-18-1 tert-butyl (8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacen-3-yl)acetate 
• 1269636-25-0 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 
• 1269636-17-0 methyl (8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacen-3-yl)acetate 
• 1269636-21-6 diethyl (8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacen-3-yl)malonate 
• 1269636-20-5 3-phenacyl-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1269636-19-2 8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1395897-66-1 3,5-diphenyl-8-(2,6-dichlorophenyl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1395897-59-2 3-phenyl-8-(2,6-dichlorophenyl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1395897-62-7 3-mesityl-8-(2,6-dichlorophenyl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 1395897-60-5 3-(4-methoxyphenyl)-8-(2,6-dichlorophenyl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 

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

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