1269636-19-2

Upstream product

• 1165898-88-3 5-(2,6-Dichlorophenyl)dipyrromethene 
• 1269636-16-9 8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 598-31-2 1-bromoacetone 
• 83-38-5 2,6-dichlorobenzaldehyde 
• 194796-34-4 (2,6-dichlorophenyl)dipyrrol-2-ylmethane 

Relevant academic research and scientific papers

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.