93463-59-3

Upstream product

• 606-31-5 2,6-dinitrobenzaldehyde 
• 93341-76-5 ethyl 3-butyl-4-methyl-1H-pyrrole-2-carboxylate 
• 93341-73-2 benzyloxycarbonyl-2 methyl-3 butyl-4 ethoxycarbonyl-5 pyrrole 
• 93341-72-1 benzyloxycarbonyl-2 dimethyl-3,5 butyl-4 pyrrole 
• 93341-74-3 ethoxycarbonyl-2 butyl-3 methyl-4 carboxyl-5 pyrrole 
• 93341-75-4 ethoxycarbonyl-2 butyl-3 methyl-4 iodo-5 pyrrole 
• 1540-36-9 3-butylpentane-2,4-dione 
• 34549-87-6 ethyl 4-butyl-3,5-dimethylpyrrole-2-carboxylate 

Relevant academic research and scientific papers

Synthese de meso-α,γ bis(diamino-2,6 phenyl) porphyrines

The syntheses of α,γ-meso-bis(2,6 diaminophenyl) octaalkyl-porphyrins are described starting from 2,6-diacetamidophenyl-bis(2'-benzyloxycarbonyl,3'4'-dialkyl, 5'-pyrryl) methanes.The synthesis of such double-picket-fence porphyrins enables the four amino

Condensation inhabitualle d'un pyrrole et d'un benzaldehyde encombre

The condensation between 2,6-dinitrobenzaldehyde and a pyrrole does not afford a dipyrrylmethane but products which result from a duplication of the starting pyrrole or from oxydo-reduction reactions of the pyrryl-arylcarbinol 9 which arise from the condensation between one molecule of pyrrole and one molecule of aldehyde.The nitro groups of the benzaldehyde play a crucial role in these reactions.