5522-63-4 Usage
Description
COPROPORPHYRIN III TETRAMETHYL ESTER is a methyl ester derivative of Coproporphyrin III, which is a tetrapyrrole compound excreted by Rhodobacter sphaeroides. It is characterized by its purple solid appearance and is one of the main tetrapyrrole compounds secreted by this bacterium in culture.
Uses
Used in Pharmaceutical Industry:
COPROPORPHYRIN III TETRAMETHYL ESTER is used as a nutritional requirement for the development of N. brasiliensis egg to third stage larvae. It plays a crucial role in the growth and development of these organisms, making it an essential component in the pharmaceutical industry for research and development purposes.
Used in Research and Development:
COPROPORPHYRIN III TETRAMETHYL ESTER is used as a research compound for studying the properties and functions of tetrapyrrole compounds. Its unique chemical structure and properties make it an interesting subject for scientific investigation, contributing to the broader understanding of these types of compounds and their potential applications.
Used in Biochemical Studies:
COPROPORPHYRIN III TETRAMETHYL ESTER is used as a biochemical research tool to study the metabolic pathways and functions of tetrapyrrole compounds in various organisms, including Rhodobacter sphaeroides. This helps researchers gain insights into the biological processes involving these compounds and their potential applications in medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 5522-63-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5522-63:
(6*5)+(5*5)+(4*2)+(3*2)+(2*6)+(1*3)=84
84 % 10 = 4
So 5522-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C40H46N4O8/c1-21-25(9-13-37(45)49-5)33-18-31-23(3)26(10-14-38(46)50-6)34(43-31)19-32-24(4)28(12-16-40(48)52-8)36(44-32)20-35-27(11-15-39(47)51-7)22(2)30(42-35)17-29(21)41-33/h17-20,41,44H,9-16H2,1-8H3/b29-17-,30-17-,31-18-,32-19-,33-18-,34-19-,35-20-,36-20-
5522-63-4Relevant articles and documents
-
Johnson,Kay
, p. 2979,2982 (1960)
-
Mercuration Reactions of Porphyrins: New Efficient Syntheses of Harderoporphyrin and Isoharderoporphyrin
Smith, Kevin M.,Langry, Kevin C.
, p. 217 - 218 (1980)
Treatment with mercury(II) acetate of metal complexes of porphyrins bearing peripherally unsubstituted positions gives the corresponding mercurated derivatives; using the palladium-olefin reaction, this observation is exploited in the synthesis of coproporphyrin III tetramethyl ester (2), harderoporphyrin trimethyl ester (3), and isoharderoporphyrin trimethyl ester (4).
Improved Methods for the Synthesis of Porphyrin Alcohols and Aldehydes from Protoporphyrin IX Dimethyl Ester and Their Further Modification
Kahl, Stephen B.,Schaeck, John J.,Koo, Myoung-Seo
, p. 1875 - 1880 (1997)
-
Biosynthesis of Porphyrins and Related Macrocycles. Part 25. Synthesis of Analogues of Coproporphyrinogen-III and Studies of their Interaction with Copropophyrinogen-III Oxidase from Euglena gracilis
Robinson, John A.,McDonald, Edward,Battersby, Alan R.
, p. 1699 - 1710 (2007/10/02)
Analogues of coproporphyrinogen-III have been synthesized in which the propionate groups respectively on ring-A and on ring-B are modified either by homologation or esterification.Coproporphyrinogen-III oxidase from Euglena gracilis acts on the analogues which possess normal substituents on ring-A to generate a vinyl group on that ring.The enzyme does not affect the analogues in which the ring-A propionate group has been changed.Conditions have been defined for the MacDonald synthesis of porphyrins which yield products of high isomeric purity.
