744220-87-9

Usage

Structure

Contains a dioxane ring and a carboxylic acid functional group

Functional groups

Carboxylic acid, dioxane ring

Applications

a. Intermediate in the synthesis of pharmaceuticals and agrochemicals
b. Building block in the production of various polymers and materials
c. Starting material for the synthesis of more complex molecules in organic chemistry

Hazardous nature

Should be handled with care due to potential hazards if not used properly

Chemical classification

Carboxylic acid derivative

Appearance

Not specified in the provided material

Solubility

Not specified in the provided material

Melting/Boiling point

Not specified in the provided material

Reactivity

Not specified in the provided material, but generally reacts with other compounds to form new molecules through its carboxylic acid functional group

Upstream product

• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 298-12-4 Glyoxilic acid 

Downstream Products

• 744220-92-6 1-benzoyl-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 
• 1026263-50-2 (5,5-dimethyl-[1,3]dioxan-2-yl)-{5-[phenyl-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-methanol 
• 744220-89-1 1-[(5,5-dimethyl-1,3-dioxan-2-yl)carbonyl]-5-phenyldipyrromethane 

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