73869-98-4

Upstream product

• 67-56-1 methanol 
• 73869-97-3 5-Benzyloxycarbonyl-4-carboxymethyl-2-methylpyrrol-3-essigsaeure 
• 84089-81-6 benzyl 4-acetyl-3-methoxycarbonylmethyl-5-methylpyrrole-2-carboxylate 
• 73869-96-2 Methyl-5-methoxycarbonyl-4-methoxycarbonylmethyl-2-methylpyrrol-3-acetat 
• 100-51-6 benzyl alcohol 
• 123-54-6 acetylacetone 
• 124-41-4 sodium methylate 
• 162661-74-7 benzyl-3,4-di-(2-benzyloxycarbonylmethyl)-5-methyl-2-pyrrole carboxylate 
• 1830-54-2 3-oxopentanedioic acid dimethyl ester 
• 50622-72-5 4-iodo-3-methoxycarbonylmethyl-5-methyl-pyrrole-2-carboxylic acid methyl ester 
• 73869-95-1 methyl 4-acetyl-3-methoxycarbonylmethyl-5-methylpyrrole-2-carboxylate 
• 84089-80-5 Benzyl 3-(methoxycarbonyl)methyl-5-methylpyrrole-2-carboxylate 
• 50622-73-6 methyl 3-<(methoxycarbonyl)methyl>-5-methylpyrrole-2-carboxylate 

Downstream Products

• 73870-00-5 Methyl-5-benzyloxycarbonyl-4-methoxycarbonylmethyl-2-hydroxyiminomethylpyrrol-3-acetat 
• 84089-87-2 benzyl 3,4-di(2-acetoxyethyl)-5'-t-butoxycarbonyl-3'-(2-methoxycarbonylethyl)-4'-methyl-2,2'-dipyrrylmethane-5-carboxylate 
• 84089-86-1 dibenzyl 3,4-di(2-acetoxyethyl)-3',4'-dimethyl-2,2'-dipyrrylmethane-5,5'-dicarboxylate 
• 84089-88-3 benzyl 3,4-di(2-acetoxyethyl)-5'-formyl-3'-(2-methoxycarbonylethyl)-4'-methyl-2,2'-dipyrrylmethane-5-carboxylate 
• 84089-83-8 benzyl 3,4-di(2-acetoxyethyl)-5-acetoxymethylpyrrole-2-carboxylate 
• 910246-77-4 dibenzyl 3,3',4,4'-tetramethoxycarbonylmethyl-2,2'-methylenedipyrrole-5,5'-dicarboxylate 
• 73870-14-1 Methyl-2-acetoxymethyl-5-benzylcarbonyl-4-methoxycarbonylmethylpyrrol-3-acetat 
• 73869-99-5 Methyl-5-benzyloxycarbonyl-2-formyl-4-methoxycarbonylmethylpyrrol-3-acetat 

Relevant academic research and scientific papers

Synthesis and photophysical characteristics of 2,3,12,13-tetraalkylbacteriochlorins

Bacteriochlorins absorb strongly in the near-infrared spectral region and hence are of great interest across the field of photochemistry. The established de novo self-condensation of a dihydrodipyrrin-acetal has afforded stable bacteriochlorins bearing a

Chemistry of Pyrrolic Compounds. LI. Porphyrins with Electron-Withdrawing Groups in the Same Pyrrolic Ring: Preparation of a Pyridazinoporphyrin

The preparation and properties of porphyrins bearing electron-withdrawing groups in the same pyrrolic ring are described.The principal example studied is a diformylporphyrin and this has been used to prepare a porphyrin containing a fused pyridazine ring.The properties of this novel system are discussed.

Tetrapyrrole Biosynthesis, 9. - Synthesis of Protected Nor- and Homoporphobilinogen

The monopyrroles norporphobilinogen (3) and homoporphobilinogen (4) , being derivates of the biogenetic porphyrin precursor porphobilinogen (1), are of topical interest for biomimetic porphyrin syntheses.Syntheses were developed for the protected " depot