53872-58-5

Basic information

• Product Name: 3-(2-chloroethyl)-8,13,17-tris(2-methoxycarbonylethyl)-2,7,12,18-tetramethylporphyrin
• Synonyms: 3-(2-chloroethyl)-8,13,17-tris(2-methoxycarbonylethyl)-2,7,12,18-tetramethylporphyrin
• CAS NO: 53872-58-5
• Molecular Weight: 687.236
• Mol File: 53872-58-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(2-chloroethyl)-8,13,17-tris(2-methoxycarbonylethyl)-2,7,12,18-tetramethylporphyrin(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-chloroethyl)-8,13,17-tris(2-methoxycarbonylethyl)-2,7,12,18-tetramethylporphyrin(53872-58-5)
• EPA Substance Registry System: 3-(2-chloroethyl)-8,13,17-tris(2-methoxycarbonylethyl)-2,7,12,18-tetramethylporphyrin(53872-58-5)

Safety Data

• Hazardous Substances Data: 53872-58-5(Hazardous Substances Data)

Upstream product

• 1268883-87-9 C₁₇H₂₃ClN₂O₂ 
• 4792-10-3 3-{5-Formyl-2-[5-formyl-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrol-2-ylmethyl]-4-methyl-1H-pyrrol-3-yl}-propionic acid methyl ester 

Downstream Products

• 30783-27-8 3-vinyl-2,7,12,18-tetramethylporphyrin-8,13,17-tripropionic acid 
• 553-12-8 protoporphyrin IX 

Relevant articles and documents

The oxygen-independent coproporphyrinogen III oxidase HemN utilizes harderoporphyrinogen as a reaction intermediate during conversion of coproporphyrinogen III to protoporphyrinogen IX

During heme biosynthesis the oxygen-independent coproporphyrinogen III oxidase HemN catalyzes the oxidative decarboxylation of the two propionate side chains on rings A and B of coproporphyrinogen III to the corresponding vinyl groups to yield protoporphyrinogen IX. Here, the sequence of the two decarboxylation steps during HemN catalysis was investigated. A reaction intermediate of HemN activity was isolated by HPLC analysis and identified as monovinyltripropionic acid porphyrin by mass spectrometry. This monovinylic reaction intermediate exhibited identical chromatographic behavior during HPLC analysis as harderoporphyrin (3-vinyl-8,13,17-tripropionic acid-2,7,12,18- tetramethylporphyrin). Furthermore, HemN was able to utilize chemically synthesized harderoporphyrinogen as substrate and converted it to protoporphyrinogen IX. These results suggest that during HemN catalysis the propionate side chain of ring A of coproporphyrinogen III is decarboxylated prior to that of ring B. by Walter de Gruyter.