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3-anilino-4-methyl-1,5-diphenyl-5H-pyrrol-2-one is a complex organic compound with the molecular formula C23H20N2O. It is a derivative of pyrrole, a heterocyclic aromatic compound containing a nitrogen atom in the ring structure. This specific compound features an aniline group (an amino group attached to a phenyl ring) at the 3-position, a methyl group at the 4-position, and two phenyl rings at the 1 and 5 positions. The compound exhibits a keto group at the 2-position, which is characteristic of the pyrrol-2-one class of compounds. Due to its unique structure, it has potential applications in various fields, such as pharmaceuticals and materials science, as it may possess specific biological activities or chemical properties.

5468-13-3

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5468-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5468-13-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5468-13:
(6*5)+(5*4)+(4*6)+(3*8)+(2*1)+(1*3)=103
103 % 10 = 3
So 5468-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C23H20N2O/c1-17-21(24-19-13-7-3-8-14-19)23(26)25(20-15-9-4-10-16-20)22(17)18-11-5-2-6-12-18/h2-16,22,24H,1H3

5468-13-3Downstream Products

5468-13-3Relevant academic research and scientific papers

REACTION OF α-KETOGLUTARIC ACID WITH SCHIFF BASES

Gein, V. L.,Popov, A. V.,Andreichikov, Yu. S.

, p. 2291 - 2295 (2007/10/02)

1,5-Diaryl-3-arylamino-4-carboxymethyl-2,5-dihydropyrrol-2-ones were synthesized in the reaction of α-ketoglutaric acid with Schiff bases. Their hydrolysis in concentrated hydrochloric acid results in 1,5-diaryl-3-hydroxy-4-carboxymethyl-2,5-dihydropyrrol-2-ones. These latter are converted into the initial compounds when treated with arylamines. The heating of 1,5-diaryl-4-methoxycarbonyl-2,5-dihydropyrrol-2-ones and their 3-arylamino derivatives above the melting point leads to their decarboxylation, while the treatment with diphenyldiazomethane converts them into the corresponding benzhydryl ethers.

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