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1-(4-methoxyphenyl)-2,5-dimethyl-3-phenyl-1H-pyrrole is a complex organic compound with the molecular formula C20H19NO. 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 structure of 1-(4-methoxyphenyl)-2,5-dimethyl-3-phenyl-1H-pyrrole is characterized by a pyrrole ring with two methyl groups at positions 2 and 5, a phenyl group at position 3, and a 4-methoxyphenyl group at position 1. 1-(4-methoxyphenyl)-2,5-dimethyl-3-phenyl-1H-pyrrole is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties and structural features.

3771-59-3

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3771-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3771-59-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3771-59:
(6*3)+(5*7)+(4*7)+(3*1)+(2*5)+(1*9)=103
103 % 10 = 3
So 3771-59-3 is a valid CAS Registry Number.

3771-59-3Downstream Products

3771-59-3Relevant academic research and scientific papers

Dearomatization Strategy for the Synthesis of Arylated 2H-Pyrroles and 2,3,5-Trisubstituted 1H-Pyrroles

Polák, Peter,Tobrman, Tomá?

, p. 4608 - 4611 (2017)

The first high-yielding route to arylated 2H-pyrroles was developed. The methodology utilizes 2,5-disubstituted pyrroles that are metalated, and the aryl substituents are introduced by a palladium-catalyzed cross-coupling reaction. The prepared pyrroles can be rearranged to 2,3,5-trisubstituted pyrroles under acidic conditions. Attempts to convert the 2,3,5-trisubstituted pyrroles to 2,3,4,5-tetrasubstituted pyrroles by the dearomatization rearrangement strategy were unsuccessful.

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