744220-89-1

Upstream product

• 107798-98-1 5-phenyldipyrromethane 
• 744220-88-0 5,5-dimethyl-[1,3]dioxane-2-carbothioic acid S-pyridin-2-yl ester 
• 925-90-6 ethylmagnesium bromide 
• 744220-87-9 5,5-dimethyl-1,3-dioxane-2-carboxylic acid 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 

Downstream Products

• 744220-92-6 1-benzoyl-9-[(5,5-dimethyl-1,3-dioxan-2-yl)carbonyl]-5-phenyldipyrromethane 
• 1026263-50-2 (5,5-dimethyl-[1,3]dioxan-2-yl)-{5-[phenyl-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-methanol 
• 946832-12-8 1-bromo-9-[(5,5-dimethyl-1,3-dioxan-2-yl)carbonyl]-5-phenyldipyrromethane 
• 1027954-63-7 (5,5-dimethyl-[1,3]dioxan-2-yl)-(5-{[5-(hydroxy-phenyl-methyl)-1H-pyrrol-2-yl]-phenyl-methyl}-1H-pyrrol-2-yl)-methanol 

Relevant academic research and scientific papers

Route to formyl-porphyrins

A method of making a 5-formylporphyrin, comprises the steps of: condensing a 5-acetaldipyrromethane with a dipyrromethane-1,9-dicarbinol to produce a porphyrin having an acetal group substituted thereon at the 5 position; and then hydrolyzing said porphyr

A new route to meso-formyl porphyrins

Prior syntheses of porphyrins bearing meso-formyl groups have generally employed the Vilsmeier formylation of an acid-resistant copper or nickel porphyrin. A new approach for the synthesis of free base porphyrins bearing one or two (cis or trans) meso-for