74839-10-4

Basic information

• Product Name: 1H-Pyrrole-3-propanoic acid, 5,5'-methylenebis[4-methyl-2-[(phenylmethoxy)carbonyl]-, dimethyl ester
• CAS NO: 74839-10-4
• Molecular Formula: C35H38N2O8
• Molecular Weight: 614.695
• Mol File: 74839-10-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole-3-propanoic acid, 5,5'-methylenebis[4-methyl-2-[(phenylmethoxy)carbonyl]-, dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-3-propanoic acid, 5,5'-methylenebis[4-methyl-2-[(phenylmethoxy)carbonyl]-, dimethyl ester(74839-10-4)
• EPA Substance Registry System: 1H-Pyrrole-3-propanoic acid, 5,5'-methylenebis[4-methyl-2-[(phenylmethoxy)carbonyl]-, dimethyl ester(74839-10-4)

Safety Data

• Hazardous Substances Data: 74839-10-4(Hazardous Substances Data)

Upstream product

• 18711-59-6 4-methyl-1H-pyrrole-2-carboxylic acid 
• 51671-81-9 2-benzoyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methyl-5-(acetoxymethyl)pyrrole 
• 40611-90-3 4,N,N-trimethylpyrrole-2-carboxamide 

Downstream Products

• 5522-66-7 3,3'-(3,7,12,17-tetramethyl-8,13-divinyl-21H,23H-porphine-2,18-diyl)-bis-propionic acid dimethyl ester 

Relevant articles and documents

Synthetic and Biosynthetic Studies of Porphyrins. Part 9. Synthesis of Isocoproporphyrin, Dehydroisocoproporphyrin, and De-ethylisocopropophyrin

The title compounds, which were extracted by patients suffering from porphyria cutanea tarda or rats poisoned with hexachlorobenzene have been synthesized by the b-oxobilane route.Isocoproporphyrin tetramethyl ester (7a) were prepared from pyrromethanes c

Biosynthesis of Porphyrins and Related Macrocycles. Part 13. Structure of the Protoporphyrin Isomer derived from Coproporphyrinogen lV by the Action of Beef-Liver Coproporphyrinogenase: Synthesis of Protoporphyrin Xlll

Coproporphyrinogen lV (8) is synthesised and is oxidatively decarboxylated by coproporphyrinogenase from beef-liver to produce, after aromatisation, a porphyrin proved to be protoporphyrin Xlll (11) by spectroscopy and by unambiquous synthesis; the synthesis route is described.A monovinylporphyrin, derived from an intermediate for the conversion (8) -> (11), is also isolated.The importance of these results for earlier biosynthetic studies with pyrromethanes is discussed.