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1H-Pyrrole-3-carbonitrile, 5-methyl-2,4-diphenyl- is a chemical compound with the molecular formula C18H14N2. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with one nitrogen atom and four carbon atoms. In this specific compound, the pyrrole ring is substituted with a methyl group at the 5-position and two phenyl groups at the 2 and 4 positions. The presence of a carbonitrile group at the 3-position further modifies the structure. 1H-Pyrrole-3-carbonitrile, 5-methyl-2,4-diphenyl- is known for its potential applications in the synthesis of various pharmaceuticals and organic materials due to its unique structure and properties.

86297-00-9

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86297-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86297-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,9 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86297-00:
(7*8)+(6*6)+(5*2)+(4*9)+(3*7)+(2*0)+(1*0)=159
159 % 10 = 9
So 86297-00-9 is a valid CAS Registry Number.

86297-00-9Downstream Products

86297-00-9Relevant academic research and scientific papers

Addition d'azlactones ylures d'azomethine potentiels a quelques alcenes electrophiles, en milieu anhydride acetique : obtention de pyrrolines-2 et de pyrroles N-acetyles

Yebdri, Okacha,Texier, Fernand

, p. 195 - 201 (2007/10/02)

Azlactones, potential azomethin-ylids, are prepared in situ acetic anhydride from the corresponding α-amino acid, and their addition to electrophilic alkenes RCH=C(X)(Y) leads to N-acetyl Δ2-pyrroline.If X=Y=CN, the pyrroline eliminates HCN and produces a pyrrole.If R=H (acrylic and methacrylic esters and nitriles) the hydrolytic openchain products are obtained.

ORIENTATION DE LA CYCLOADDITION D'OXAZOLONES MESOIONIQUES AUX ALCENES

Yebdri, Okacha,Henri-Rousseau, Olivier,Texier, Fernand

, p. 369 - 372 (2007/10/02)

The regioselectivity of the cycloaddition of mesoionic oxazolones to alkenes has been found to be markedly dependent on the substituent groups present and an explanation is proposed.

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