131353-85-0

Upstream product

• 131353-80-5 (4-Bromphenyl)bis(5-carboxy-4-ethyl-3-methyl-2-pyrryl)methan 
• 131353-74-7 Diethyl 5-(4-bromophenyl)-2,8-diethyl-3,7-dimethyldihydrodipyrrin-1,9-dicarboxylate 
• 4949-58-0 2-(ethyloxycarbonyl)-3-ethyl-4-methylpyrrole 
• 1122-91-4 4-bromo-benzaldehyde 

Downstream Products

• 448-70-4 etioporphyrin II 
• 131353-94-1 (5Z,10Z,14Z,19Z)-5-(4-Bromo-phenyl)-2,8,13,17-tetraethyl-3,7,12,18-tetramethyl-porphyrin 
• 131353-93-0 5-(4-Bromphenyl)-15-(2,5-dimethoxyphenyl)-2,8,12,18-tetraethyl-3,7,13,17-tetramethylporphin 
• 131353-88-3 5,15-Bis(2,5-dimethoxyphenyl)-2,8,12,18-tetraethyl-3,7,13,17-tetramethylporphin 
• 179690-80-3 zinc(II) 5-(4-bromophenyl)-2,8-diethyl-13,17-bis(methoxycarbonylethyl)-3,7,12,18-tetramethylporphyrin 

Relevant academic research and scientific papers

Nucleoside adducts of vinylporphyrins and vinylchlorins

Ethene-linked nucleoside derivatives of porphyrins and chlorins have been synthesized by palladium-catalysed coupling between acetylated 5-chloromercuriuridine and various vinylporphyrins and vinylchlorins. The formation of both the trans- (e.g. 22, 24, 2

Synthesis of 5,15-Diaryl-Substituted Porphyrins by Aminomethylation of Bis(4-ethyl-3-methyl-2-pyrryl)phenylmethanes

The synthesis of unsymmetrically diarylsubstituted porphyrins 11a-g (yields 5-19 percent) is described.Aminomethylation of dipyrromethane 6a with Mannich reagent 9 in acetonitrile leads to the intermediate 10, which is directly converted into the porphyri