17484-82-1

Basic information

• Product Name: benzyl 5-dimethylamido-3,4'-dimethyl-4,3'-bis(2'-methoxycarbonylethyl)-pyrromethane-5'-carboxylate
• CAS NO: 17484-82-1
• Molecular Weight: 551.64
• Mol File: 17484-82-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl 5-dimethylamido-3,4'-dimethyl-4,3'-bis(2'-methoxycarbonylethyl)-pyrromethane-5'-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 5-dimethylamido-3,4'-dimethyl-4,3'-bis(2'-methoxycarbonylethyl)-pyrromethane-5'-carboxylate(17484-82-1)
• EPA Substance Registry System: benzyl 5-dimethylamido-3,4'-dimethyl-4,3'-bis(2'-methoxycarbonylethyl)-pyrromethane-5'-carboxylate(17484-82-1)

Safety Data

• Hazardous Substances Data: 17484-82-1(Hazardous Substances Data)

Upstream product

• 111017-83-5 ethyl 3-(2-ethoxycarbonylethyl)-4-methoxycarbonylmethyl-5-methylpyrrole-2-carboxylate 
• 111017-82-4 ethyl 5-methoxycarbonylmethyl-4,6-dioxoheptanoate 
• 50622-64-5 benzyl 3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethyl-5-methylpyrrole-2-carboxylate 
• 31896-84-1 5-chlorocarbonyl-4-(2-methoxycarbonyl-ethyl)-3-methyl-pyrrole-2-carboxylic acid benzyl ester 
• 74839-00-2 methyl 5-methyl-4,6-dioxoheptanoate 
• 60205-10-9 3-(2-dimethylcarbamoyl-5-iodo-4-methyl-pyrrol-3-yl)-propionic acid methyl ester 
• 37538-30-0 5-dimethylcarbamoyl-4-(2-methoxycarbonyl-ethyl)-3-methyl-pyrrole-2-carboxylic acid benzyl ester 
• 20303-31-5 benzyl 4-(2-methoxycarbonylethyl)-3,5-dimethylpyrrole-2-carboxylate 
• 39265-95-7 methyl 3-acetyl-4-oxopentanoate 
• 60204-90-2 5-dimethylamido-4-(2'-methoxycarbonylethyl)-3-methylpyrrole 
• 50622-67-8 5-acetoxymethyl-3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-pyrrole-2-carboxylic acid benzyl ester 
• 859-38-1 benzyl 5-acetoxymethyl-4-(2-methoxycarbonylethyl)-3-methylpyrrole-2-carboxylate 

Relevant articles and documents

Synthetic and Biosynthetic Studies of Porphyrins. Part 8. Synthese of Hepta-, Hexa-, and penta-carboxylic Porphyrins Related to Urophorphin-I

The title porphyrins of interest as abnormal metabolits in porphyrins biosynthesis, have been synthesized by the Fischer, and b-oxobilane routes, and compared with the naturally derived materials.Enzymic experiments have shown that the conversion of uropo