1384510-08-0

Upstream product

• 625-82-1 2,4-dimethyl-1H-pyrrole 
• 100-83-4 meta-hydroxybenzaldehyde 

Downstream Products

• 1434003-47-0 4,4-difluoro-2,6-diiodo-1,3,5,7-tetramethyl-8-(3′-hydroxy-4′-iodophenyl)-4-bora-3a,4a-diaza-s-indacene 
• 2534-93-2 3,5,3',5'-tetramethyl-1H,2'H-2,2'-methanylylidene-bis-pyrrole 
• 1384510-09-1 1,3,5,7-tetramethyl-8-(3-hydroxyphenyl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 21658-70-8 4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene 

Relevant academic research and scientific papers

Synthesis and photo-physical properties of a series of BODIPY dyes

A series of 39 boron-dipyrrolylmethenes (BODIPYs) have been synthesized and characterized. Their spectroscopic properties, degree of lipophilicity, chemical stability under irradiation, and singlet-oxygen generation rate have also been studied. These compounds differ in the presence of ethyl groups (group A), hydrogens (group B) or iodines (group C) on the 2,6 positions; these appendices confer particular characteristics to each group. The presence of an aromatic substituent or hydrogen on the indacene 8 position produces 13 different molecules of each group. Besides the effects exerted by the group or atom on the 2,6 positions, the substituent on the 8 position exerts a further effect on the physico-chemical parameters, thus the desired properties of BODIPYs, concerning fluorescence, lipophilicity, and singlet oxygen production can be modulated accordingly.