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ethyl 4-(4-methylphenyl)pyrrole-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127572-60-5

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127572-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127572-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,7 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127572-60:
(8*1)+(7*2)+(6*7)+(5*5)+(4*7)+(3*2)+(2*6)+(1*0)=135
135 % 10 = 5
So 127572-60-5 is a valid CAS Registry Number.

127572-60-5Relevant academic research and scientific papers

One-pot synthesis of pyrroles using a titanium-catalyzed multicomponent coupling procedure

Pasko, Cody M.,Dissanayake, Amila A.,Billow, Brennan S.,Odom, Aaron L.

, p. 1168 - 1176 (2016/02/16)

A simple one-pot procedure for the production of 2-carboxylpyrroles with 4-alkyl, 5-alkyl, 4-aryl, 4-aryl-5-alkyl, or 3,4-diaryl substitution patterns is presented. The procedure involves the titanium-catalyzed multicomponent coupling of alkynes, primary amines and isonitriles to give 1,3-diimines in situ; the multicomponent product is then treated with the ethyl ester of glycine hydrochloride to give the NH-pyrrole. The reaction can be carried out with the neutralized glycine ester or with the hydrochloride salt using DBU as a base. Yields of pyrrole based on starting alkyne varied from 25 to 65% over the one pot procedure, and in most cases only one regioisomer of the product is observed. Further, it is proposed that the regioselectivities of the reactions are a result of rate-determining ring closure after relatively fast transimination with glycine ethyl ester.

Nano-copper catalysed highly regioselective synthesis of 2,4-disubstituted pyrroles from terminal alkynes and isocyanides

Tiwari, Dipak Kumar,Pogula, Jaya,Sridhar,Tiwari, Dharmendra Kumar,Likhar, Pravin R.

, p. 13646 - 13649 (2015/09/02)

Nano-copper(0) stabilized on alumina prepared from Cu-Al hydrotalcite has been reported for completely regioselective synthesis of 2,4-disubstituted pyrroles from unactivated terminal aromatic/aliphatic alkynes and isocyanides. The reaction is operational

Application of 2-Substituted Vinamidinium Salts to the Synthesis of 2,4-Disubstituted Pyrroles

Gupton, John T.,Krolikowski, Dale A.,Yu, Richard H.,Riesinger, Steve W.,Sikorski, James A.

, p. 4735 - 4740 (2007/10/02)

A variety of 2-substituted vinamidinium salts react with α-amino acid esters under basic conditions to produce 2-carbethoxy-4-substituted-pyrroles in good yield.The overall process represents a short and efficient synthesis of highly functionalized pyrrol

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