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5-methyl-3,4-diphenyl-1H-pyrrole-2-carboxylic acid ethyl ester is a complex organic compound with the molecular formula C18H17NO2. It is a derivative of pyrrole, a heterocyclic aromatic organic compound containing a nitrogen atom in the ring. The structure of 5-methyl-3,4-diphenyl-1H-pyrrole-2-carboxylic acid ethyl ester features a pyrrole ring with a methyl group at the 5-position, two phenyl groups at the 3 and 4 positions, and a carboxylic acid group at the 2-position, which is further esterified with an ethyl group. 5-methyl-3,4-diphenyl-1H-pyrrole-2-carboxylic acid ethyl ester is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and properties. It is typically synthesized through multi-step organic reactions and is used as an intermediate in the preparation of more complex molecules.

3651-12-5

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3651-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3651-12-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3651-12:
(6*3)+(5*6)+(4*5)+(3*1)+(2*1)+(1*2)=75
75 % 10 = 5
So 3651-12-5 is a valid CAS Registry Number.

3651-12-5Relevant academic research and scientific papers

2-Amidopyrroles and 2,5-diamidopyrroles as simple anion binding Agents

Gale,Camiolo,Tizzard,Chapman,Light,Coles,Hursthouse

, p. 7849 - 7853 (2001)

Four new 2-amidopyrroles and 2,5-diamidopyrroles have been synthesized and their anion complexation properties investigated. The crystal structures of these receptors have been elucidated and reveal hydrogen bonding in the solid state leading to dimer and network formation. Selectivity for oxo-anions has been demonstrated by 1H NMR titration techniques.

Further observations on conformational and substituent effects in acid-catalyzed "3 + 1" cyclizations of tripyrranes with aromatic dialdehydes

Lash, Timothy D.,Bergman, Katrina M.

, p. 9774 - 9783 (2013/01/15)

Tripyrranes with tert-butyl and phenyl substituents have been prepared and used to synthesize oxybenziporphyrins, oxypyriporphyrins, benzocarbaporphyrins, and azuliporphyrins with phenyl and tert-butyl substituents via a "3 + 1" methodology. The proton NM

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