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N-phenyl-1H-pyrrole-1-carboxamide is a chemical compound with the molecular formula C11H10N2O. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with two carbon atoms and two nitrogen atoms. The N-phenyl group attached to the pyrrole ring provides additional stability and reactivity to the molecule. N-phenyl-1H-pyrrole-1-carboxamide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in materials science for the development of new polymers and dyes. Its unique structure and properties make it an interesting target for researchers in organic chemistry and medicinal chemistry.

4778-72-7

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4778-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4778-72-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,7 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4778-72:
(6*4)+(5*7)+(4*7)+(3*8)+(2*7)+(1*2)=127
127 % 10 = 7
So 4778-72-7 is a valid CAS Registry Number.

4778-72-7Downstream Products

4778-72-7Relevant academic research and scientific papers

Highly stereoselective ruthenium(II)-catalyzed direct C2- syn -alkenylation of indoles with alkynes

Zhang, Wei,Wei, Jun,Fu, Shaomin,Lin, Dongen,Jiang, Huanfeng,Zeng, Wei

supporting information, p. 1349 - 1352 (2015/03/30)

A carboamide-directed ruthenium-catalyzed C2-hydroindolation of alkynes has been described. This transformation provides a rapid access to free (N-H) C2-syn-alkenylated indole derivatives with the assistance of copper(II) salts, in which the directing group is removed via a one-pot process.

A simple direct phosgeneless route to N-heteroaryl unsymmetrical ureas

Carafa, Marianna,Mele, Valentina,Quaranta, Eugenio

experimental part, p. 217 - 225 (2012/03/26)

A new simple approach to the synthesis of unsymmetrical ureas HetNC(O)NRR′ (HetNH = pyrrole, indole, carbazole; R, R′ = H, alkyl, aryl) has been explored, which involves the direct reaction of the N-phenoxycarbonyl derivatives of pyrrole, indole and carba

Oxidation of N-Acyl-Pyrrolidines and -Piperidines with Iron(II)-Hydrogen Peroxide and an Iron Complex-Molecular Oxygen

Murata, Satoru,Miura, Masahiro,Nomura, Masakatsu

, p. 1259 - 1262 (2007/10/02)

The reactions of N-acyl-pyrrolidines (1a-c) and -piperidines (1d-f) with Fe(II)-hydrogen peroxide in aqueous 95percent acetonitrile gave the corresponding pyrrolidin-2-ones (2a-c) and piperidin-2-ones (2d-f).The lactams (2a-f) were also the products in the oxidation of (1a-f) with molecular oxygen in the presence of an iron complex, either or , in aqueous 90percent pyridine.

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