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Propanamide, N-2-cyclohexen-1-yl-2,2-dimethyl-, also known as 2-cyclohexen-1-yl-N,N-dimethyl-2-propanamide, is an organic compound with the chemical formula C11H19NO. It is a derivative of propanamide, featuring a cyclohexenyl group attached to the nitrogen atom. Propanamide, N-2-cyclohexen-1-yl-2,2-dimethyl- is characterized by its unique structure, which includes a cyclohexene ring and a dimethyl group on the nitrogen, contributing to its specific chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research.

4981-52-6

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4981-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4981-52-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,8 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4981-52:
(6*4)+(5*9)+(4*8)+(3*1)+(2*5)+(1*2)=116
116 % 10 = 6
So 4981-52-6 is a valid CAS Registry Number.

4981-52-6Downstream Products

4981-52-6Relevant academic research and scientific papers

Silver Salt-Mediated Allylation Reactions Using Allyl Bromides

Xiong, Xiaodong,Wong, Jonathan,Yeung, Ying-Yeung

supporting information, p. 6974 - 6982 (2021/05/06)

A facile, efficient, and chemoselective synthesis of allylic amides has been developed. Allyl bromides were used as the precursors activated by silver triflate. A Ritter-type reaction readily proceeded to give various allyl amides under mild conditions. The reaction protocol was also applicable to different nucleophilic partners to give a wide range of allyl-substituted products in the absence of a base.

cis- and trans-Stereoselective Epoxidation of N-Protected 2-Cyclohexen-1-ylamines

O'Brien, Peter,Childs, Amanda C.,Ensor, Gareth J.,Hill, Cheryl L.,Kirby, Jonathan P.,Dearden, Michael J.,Oxenford, Sally J.,Rosser, Clare M.

, p. 4955 - 4957 (2007/10/03)

(Equation Presented) The first systematic study of the cis and trans stereoselectivity in the m-CPBA epoxidation of N-protected cyclic allylic amines has been completed. Mono-N-protected systems gave epoxides with cis stereochemistry (amides are better ci

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