75630-48-7

Basic information

• Product Name: dibenzyl 3,3'-bismethyl-4,4'-bis-(2-hydroxyethyl)pyrromethane-5,5'-dicarboxylate
• CAS NO: 75630-48-7
• Molecular Weight: 530.621
• Mol File: 75630-48-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: dibenzyl 3,3'-bismethyl-4,4'-bis-(2-hydroxyethyl)pyrromethane-5,5'-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dibenzyl 3,3'-bismethyl-4,4'-bis-(2-hydroxyethyl)pyrromethane-5,5'-dicarboxylate(75630-48-7)
• EPA Substance Registry System: dibenzyl 3,3'-bismethyl-4,4'-bis-(2-hydroxyethyl)pyrromethane-5,5'-dicarboxylate(75630-48-7)

Safety Data

• Hazardous Substances Data: 75630-48-7(Hazardous Substances Data)

Upstream product

• 75630-47-6 dibenzyl 3,3'-dimethyl-4,4'-bis(methoxycarbonylmethyl)pyrromethane-5,5'-dicarboxylate 
• 75630-44-3 1-Iodomethyl-3-methoxycarbonylmethyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid methyl ester 
• 75630-45-4 methyl 4,5-dimethyl-3-(methoxycarbonylmethyl)pyrrole-2-carboxylate 
• 50622-72-5 4-iodo-3-methoxycarbonylmethyl-5-methyl-pyrrole-2-carboxylic acid methyl ester 
• 62562-72-5 benzyl 3-(benzyloxycarbonylmethyl)-4,5-dimethylpyrrole-2-carboxylate 
• 57907-68-3 benzyl 3-(methoxycarbonylmethyl)-4,5-dimethylpyrrole-2-carboxylate 
• 75630-46-5 benzyl 5-acetoxymethyl-3-(methoxycarbonylmethyl)-4-methylpyrrole-2-carboxylate 
• 50622-73-6 methyl 3-<(methoxycarbonyl)methyl>-5-methylpyrrole-2-carboxylate 

Downstream Products

• 75747-97-6 dibenzyl 4,4'-bis(2-acetoxyethyl)-3,3'-dimethylpyrromethane-5,5'-dicarboxylate 

Relevant articles and documents

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.