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N-(2-(piperidin-1-yl)ethyl)benzamide is a chemical compound with the molecular formula C14H22N2O. It is a derivative of benzamide, featuring a piperidine ring attached to the ethyl group, which in turn is connected to the benzene ring through an amide linkage. N-(2-(piperidin-1-yl)ethyl)benzamide is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. It is characterized by its ability to form hydrogen bonds and its potential to interact with biological targets, making it a subject of interest for medicinal chemistry research. The compound's structure allows for further functionalization and modification, which can lead to the development of new therapeutic agents with specific pharmacological properties.

4380-82-9

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4380-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4380-82-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4380-82:
(6*4)+(5*3)+(4*8)+(3*0)+(2*8)+(1*2)=89
89 % 10 = 9
So 4380-82-9 is a valid CAS Registry Number.

4380-82-9Downstream Products

4380-82-9Relevant academic research and scientific papers

3,6-Di(pyridin-2-yl)-1,2,4,5-tetrazine (pytz) catalysed metal-free amide bond formation from thioacids and amines at room temperature

Samanta, Suvendu,Ray, Shounak,Bhaduri, Samanka Narayan,Samanta, Partha Kumar,Biswas, Papu

supporting information, (2020/08/10)

A 3,6-di(pyridin-2-yl)-1,2,4,5-tetrazine (pytz) catalysed efficient, mild and metal-free method has been developed for direct amide bond synthesis from simple thioacids and amines as starting materials. This methodology is useful for aromatic, aliphatic, and heteroaromatic thioacids as well as primary, secondary, heterocyclic, and even functionalized amines. A wide substrates scope, operationally mild conditions, and acylation of amines without affecting other functional groups such as alcohols, esters, carbodithioates, among others make this strategy very attractive and practical.

High throughput 'catch-and-release' synthesis within spatially discrete gel arrays

Boehner, Christine M.,Marsden, David M.,Sore, Hannah F.,Norton, David,Spring, David R.

supporting information; experimental part, p. 5930 - 5932 (2010/11/21)

A tetrafluorophenol acrylamide monomer unit was synthesised, co-polymerised and grafted onto a glass slide to form individual gel spots. As a proof of principle study, a small library of amides was rapidly synthesised within these gel spots using 'catch-and-release' chemistry, including the biologically interesting quorum sensing acyl-homoserine lactones. The tetrafluorophenol acrylamide gel provides an efficient platform to synthesise and screen small molecules for biological activity.

A mild chemospecific reductive dehalogenation of ethylaminobenzamides with lithium aluminum hydride

Hendrix, James A.,Stefany, David W.

, p. 6749 - 6752 (2007/10/03)

A mild reduction of ortho-fluoro benzamides was discovered using LAH. The reaction proceeds cleanly and in moderate yields. The scope of the reaction is explored and a mechanism is proposed. A two carbon spacer between the amide and a 3°amine is optimal for this chelation controlled reaction.

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