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1-[1-(4-methoxybenzyl)-2-methyl-4-(thiophen-2-yl)-1H-pyrrol-3-yl]-ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1208334-71-7

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1208334-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1208334-71-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,3,3 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1208334-71:
(9*1)+(8*2)+(7*0)+(6*8)+(5*3)+(4*3)+(3*4)+(2*7)+(1*1)=127
127 % 10 = 7
So 1208334-71-7 is a valid CAS Registry Number.

1208334-71-7Downstream Products

1208334-71-7Relevant academic research and scientific papers

β-Cyclodextrin as a recyclable catalyst: Aqueous phase one-pot four-component synthesis of polyfunctionalized pyrroles

Konkala, Karnakar,Chowrasia, Rakhi,Manjari, Padma S.,Domingues, Nelson L. C.,Katla, Ramesh

, p. 43339 - 43344 (2016)

An elegant, mild and straightforward methodology was explored for the first time towards the synthesis of polyfunctionalized pyrroles using β-cyclodextrin as a reusable supramolecular catalyst in aqueous medium. The present method provides various diversely substituted pyrroles from the commercially available synthons in good to excellent yields. The advantages of this novel protocol are use of environmentally benign reaction medium and recyclability of β-cyclodextrin over the existing methods.

Iron(III)-catalyzed four-component coupling reaction of 1,3-dicarbonyl compounds, amines, aldehydes, and nitroalkanes: A simple and direct synthesis of functionalized pyrroles

Maiti, Sukhendu,Biswas, Srijit,Jana, Umasish

experimental part, p. 1674 - 1683 (2010/05/01)

Chemical Equation Represented A simple, convenient, and multicomponent coupling strategy for the synthesis of highly functionalized pyrroles catalyzed by iron(III) salts has been developed. This strategy demonstrated fourcomponent coupling reactions of 1,3-dicarbonyl compounds, amines, aromatic aldehydes, and nitroalkanes without an inert atmosphere. This methodology provides an alternative approach for easy access of highly substituted pyrroles in moderate to very good yields using four simple and readily available building blocks via one-pot tandem reaction. Notably, this method is very cheap, straightforward, and environmentally friendly compared to the existing methods.

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