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2,5-diphenyl-1H-pyrrol-1-amine is an organic compound with the molecular formula C17H16N2. It is a derivative of pyrrole, a heterocyclic aromatic compound consisting of a five-membered ring with two carbon atoms and two nitrogen atoms. The molecule features two phenyl groups attached to the second and fifth carbon atoms of the pyrrole ring, and an amino group (-NH2) at the first position. 2,5-diphenyl-1H-pyrrol-1-amine is known for its potential applications in the synthesis of various pharmaceuticals and dyes due to its unique structure and reactivity. It is typically synthesized through chemical reactions involving pyrrole and phenyl-containing compounds, and its properties can be further modified by substituting different functional groups or altering the positions of the phenyl groups on the pyrrole ring.

786-98-1

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786-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 786-98-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 786-98:
(5*7)+(4*8)+(3*6)+(2*9)+(1*8)=111
111 % 10 = 1
So 786-98-1 is a valid CAS Registry Number.

786-98-1Relevant academic research and scientific papers

Oxalohydrazide Ligands for Copper-Catalyzed C?O Coupling Reactions with High Turnover Numbers

Ray, Ritwika,Hartwig, John F.

supporting information, p. 8203 - 8211 (2021/03/08)

Here, we report a class of ligands based on oxalohydrazide cores and N-amino pyrrole and N-amino indole units that generates long-lived copper catalysts for couplings that form the C?O bonds in biaryl ethers. These Cu-catalyzed coupling of phenols with aryl bromides occurred with turnovers up to 8000, a value which is nearly two orders of magnitude higher than those of prior couplings to form biaryl ethers and nearly an order of magnitude higher than those of any prior copper-catalyzed coupling of aryl bromides and chlorides. This ligand also led to copper systems that catalyze the coupling of aryl chlorides with phenols and the coupling of aryl bromides and iodides with primary benzylic and aliphatic alcohols. A wide variety of functional groups including nitriles, halides, ethers, ketones, amines, esters, amides, vinylarenes, alcohols and boronic acid esters were tolerated, and reactions occurred with aryl bromides in pharmaceutically related structures.

Conversion of pyrroles into bi-1,2,5-thiadiazoles: A new route to biheterocycles

Duan, Xiao-Guang,Rees, Charles W.

, p. 3189 - 3196 (2007/10/03)

Trithiazyl trichloride 1 converts 1,2,5-triphenylpyrrole 5 into its 3,4-dichloro derivative together with the isothiazole imine 6 and the imine hydrolysis product, the ketone 3. The best yield of the isothiazole 6 is obtained in the presence of 4 A molecular sieves (Table 1). Conversion of the pyrrole 5 into the isothiazole 6 is exactly analogous to the reaction of 1 with 2,5-diphenyl-furan and -thiophene. Other N-aryl and the related 2,5-diphenylpyrroles 8 give similar results (Table 2). However, 1-methyl-2,5-diphenylpyrrole 11 reacts with 1 in an entirely different way to give 4,4′-diphenyl-3,3′-bi-1,2,5-thiadiazole 12, in which two thiadiazole rings have been fused onto the pyrrole and the CH3N unit has been excised as HCN. The same product 12 is formed, in similar yields, by reaction of 1 with 1,4-diphenylbuta-1, 3-diyne and 1,4-diphenylbut-1-en-3-yne. Other N-alkyl 2,5-diphenylpyrroles 16 react similarly (Table 3), giving the best yield (70%) of bi-thiadiazole 12 in the presence of 4 A molecular sieves (Table 4). 1-Methyl- and 1-ethyl-3,4-dibromo-2,5-diphenylpyrrole also give 12, together with 3-(benzoyldichloromethyl)-4-phenyl-1,2,5-thiadiazole 21 in high combined yield. The formation of bi-1,2,5-thiadiazole 12 from N-alkylpyrroles represents a new dissection of the pyrrole ring and a new and very short route to an aromatic biheterocyclic system. Mechanisms which rationalise the different pathways observed are proposed for all of these reactions.

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