25767-20-8 Usage
Description
Coproporphyrin I Tetramethyl Ester is a tetrapyrrole compound and a methyl ester derivative of Coproporphyrin I (C685400). It is characterized by its purple-red solid appearance and is excreted by Rhodobacter sphaeroides. COPROPORPHYRIN I TETRAMETHYL ESTER serves as a nutritional requirement for the development of N. brasiliensis eggs to third-stage larvae.
Uses
Used in Pharmaceutical Industry:
Coproporphyrin I Tetramethyl Ester is used as a nutritional supplement for the development of N. brasiliensis eggs 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 Chemical Industry:
As a tetrapyrrole compound, Coproporphyrin I Tetramethyl Ester is used in the chemical industry for the synthesis of various dyes and metabolites. Its unique chemical properties and structure make it a valuable component in the development of new compounds and products.
Used in Research and Development:
Coproporphyrin I Tetramethyl Ester is also utilized in research and development for its potential applications in various fields. Its unique properties and functions make it an interesting subject for further study and exploration, potentially leading to new discoveries and innovations in science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 25767-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,6 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25767-20:
(7*2)+(6*5)+(5*7)+(4*6)+(3*7)+(2*2)+(1*0)=128
128 % 10 = 8
So 25767-20-8 is a valid CAS Registry Number.
InChI:InChI=1/C40H46N4O8/c1-21-25(9-13-37(45)49-5)33-18-30-23(3)27(11-15-39(47)51-7)35(43-30)20-32-24(4)28(12-16-40(48)52-8)36(44-32)19-31-22(2)26(10-14-38(46)50-6)34(42-31)17-29(21)41-33/h17-20,41,44H,9-16H2,1-8H3/b29-17-,30-18-,31-19-,32-20-,33-18-,34-17-,35-20-,36-19-
25767-20-8Relevant articles and documents
Studies on the tetramerization of substituted monopyrroles to type I porphyrins
Pichon-Santander,Scott
, p. 6967 - 6969 (2002)
Investigation of the tetramerization of pyrroles bearing two different electron-donating groups as substituents led to the rapid preparation under slightly acidic conditions of a porphyrin analog family with a high ratio of type I isomer for enzymatic act
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Abraham et al.
, p. 620,621,622 (1966)
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Syntheses of type-I porphyrins via monopyrrole tetramerization
Nguyen, Liem T.,Smith, Kevin M.
, p. 7177 - 7180 (2007/10/03)
Treatment of 2-[(N,N-dialkylamino)methyl]pyrrole-5-carboxylic acids (e.g. 10,12 or 11,13) in methanol with K3Fe(CN)6 gives type-I porphyrins (etioporphyrin-I 7, coproporphyrin-I tetramethyl ester 16, respectively); with pyrroles 10,12 the product 7 is contaminated with about 8% of other type-isomer(s).
Porphyrin synthesis from nitrocompounds
Ono, Noboru,Kawamura, Hisayuki,Bougauchi, Masahiro,Maruyama, Kazuhiro
, p. 7483 - 7496 (2007/10/02)
A new porphyrin synthesis starting from nitroalkenes or their equivalents is described. For example, octaethylporphyrin, coproporphyrin, porphyrin-1,2,3,4,5,6,7,8 octapropionic acid, and 2,7,12,17 tetraarylporphyrin are prepared in good yield from readily available materials such as 1-nitropropane, nitroethane, nitromethane, and aldehydes.
