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3-methyl-4-(2-methyl)propyl-1H-pyrrole-2,5-dione is a complex organic compound with the molecular formula C10H13NO2. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one nitrogen atom. The compound features a methyl group (CH3) at the 3rd position, a 2-methylpropyl group (C4H9) at the 4th position, and two carbonyl groups (C=O) at the 2nd and 5th positions. This chemical structure endows the compound with unique chemical and physical properties, making it potentially useful in various applications, such as pharmaceuticals, agrochemicals, or materials science. However, further research and characterization are needed to fully understand its properties and potential applications.

5997-62-6

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5997-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5997-62-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,9 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5997-62:
(6*5)+(5*9)+(4*9)+(3*7)+(2*6)+(1*2)=146
146 % 10 = 6
So 5997-62-6 is a valid CAS Registry Number.

5997-62-6Downstream Products

5997-62-6Relevant academic research and scientific papers

The first experimental demonstration of side chain extension of geoporphyrins in sediments

Asahina, Kenta,Asano, Junya,Kumagai, Gen,Satou, Mitsuru,Nomoto, Kouichi,Kashiyama, Yuichiro,Mita, Hajime,Nomoto, Shinya

body text, p. 1267 - 1269 (2011/02/16)

To investigate the formation process of high carbon number (>C 32) sedimentary porphyrins, heating experiments of several porphyrins were performed. Chromic acid oxidation of the heating products of protoporphyrin IX dimethyl ester afforded 2-methyl-3-npropylmaleimide as the predominant product among the side-chain extension products formed. On the other hand, saturated substituents of etioporphyrin were also extended on heating to slowly form normal and branched homologs. These results may suggest that the transalkylation of porphyrin side chains proceeds mainly by a regioselective mechanism involving alkyl radical addition to a vinyl group of chlorophylls or their diagenetic products.

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