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Ethyl 2-methyl-5-phenyl-1-(p-tolyl)-1H-pyrrole-3-carboxylate is a complex organic chemical compound with the molecular formula C20H21NO2. It is a derivative of pyrrole, a heterocyclic compound with a five-membered ring containing one nitrogen atom. The structure of ethyl 2-methyl-5-phenyl-1-(p-tolyl)-1H-pyrrole-3-carboxylate features a pyrrole ring with a methyl group at the 2-position, a phenyl group at the 5-position, and a p-tolyl group (a tolyl group with a para-methyl substitution) at the 1-position. The ethyl ester group is attached to the 3-carboxylate position, which is a key functional group in this molecule. ethyl 2-methyl-5-phenyl-1-(p-tolyl)-1H-pyrrole-3-carboxylate is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structure and functional groups.

3652-44-6

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3652-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3652-44-6 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 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3652-44:
(6*3)+(5*6)+(4*5)+(3*2)+(2*4)+(1*4)=86
86 % 10 = 6
So 3652-44-6 is a valid CAS Registry Number.

3652-44-6Downstream Products

3652-44-6Relevant academic research and scientific papers

Microwave-assisted one pot synthesis of N-substitued 2-methyl-1H-pyrrole-3-carboxylate derivatives without catalyst and solvent

Kan, Wei,Jing, Tao,Zhang, Xiao-Hong,Zheng, Yong-Jie,Chen, Lin,Zhao, Bing

, p. 2367 - 2376 (2016/03/01)

An efficient one-pot synthetic method for the N-substituted 2-methyl-1H-pyrrole-3-carboxylate derivatives has been accomplished via a microwave irradiation MCRs of various α-bromoacetophenone, amines, and ethyl acetoacetate without any solvent and catalys

Copper-mediated cross-coupling-cyclization-oxidation: A one-pot reaction to construct polysubstituted pyrroles

Liu, Pei,Liu, Jin-Ling,Wang, Heng-Shan,Pan, Ying-Ming,Liang, Hong,Chen, Zhen-Feng

supporting information, p. 4795 - 4798 (2014/05/06)

A novel and efficient procedure for the synthesis of polysubstituted pyrroles has been developed in this work. The polysubsituted pyrroles were synthesized directly from terminal alkenes, amines and β-keto esters through cross-coupling-cyclization-oxidation in the presence of a catalytic amount of cuprous chloride. This method provides a one-pot synthesis route from terminal alkenes to polysubstituted pyrroles for the first time and opens a new area in cuprous catalysis. The Royal Society of Chemistry 2014.

Three-component access to pyrroles promoted by the CAN-silver nitrate system under high-speed vibration milling conditions: A generalization of the Hantzsch pyrrole synthesis

Estevez, Veronica,Villacampa, Mercedes,Menendez, J. Carlos

, p. 591 - 593 (2013/02/22)

A sequential multicomponent process involving the high-speed vibration milling of ketones with N-iodosuccinimide and p-toluenesulfonic acid, followed by addition of a mixture of primary amines, β-dicarbonyl compounds, cerium(iv) ammonium nitrate and silver nitrate afforded polysubstituted, functionalized pyrroles. This one-pot, solid-state process can be considered as the coupling of an α-iodoketone preparation with a general version of the classical Hantzsch pyrrole synthesis.

Synthesis and antimicrobial activity of some 1,5-diaryl-2-methyl-3-carbethoxy-4-(4-methyl-piperazin-1-ylmethyl)-pyr roles and some 1,5-diaryl-2-methyl-3,4-di(4-methyl-piperazin-1-ylmethyl)-pyrroles

Cerreto,Scalzo,Villa

, p. 1735 - 1746 (2007/10/02)

The synthesis and anti-Candida activity of some 1,5-diarylpyrrole derivatives are reported and some structure-activity relationships are proposed.

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