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N-(2-cyclohexylamino-2-oxoethyl)benzamide is a complex organic compound with the molecular formula C15H20N2O2. It is a derivative of benzamide, featuring a cyclohexylamine group attached to the amide nitrogen. This chemical is characterized by its potential pharmaceutical applications, as it may exhibit properties that are relevant to drug development, such as binding to specific receptors or enzymes. The compound's structure, with a cyclohexane ring and a benzene ring connected through an amide linkage, suggests that it could have unique biochemical interactions. However, without specific details on its synthesis, properties, or uses, a more detailed summary cannot be provided. It is important to note that the potential applications and effects of N-(2-cyclohexylamino-2-oxoethyl)benzamide would need to be confirmed through rigorous scientific research and testing.

842-98-8

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842-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 842-98-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 842-98:
(5*8)+(4*4)+(3*2)+(2*9)+(1*8)=88
88 % 10 = 8
So 842-98-8 is a valid CAS Registry Number.

842-98-8Downstream Products

842-98-8Relevant academic research and scientific papers

The Ugly Duckling Metamorphosis: The Ammonia/Formaldehyde Couple Made Possible in Ugi Reactions.

Rosalba, Thaissa Pasquali F.,Kas, Samia Sayegh A.,Sampaio, Ana Beatriz S.,Salvador, Carlos Eduardo M.,Andrade, Carlos Kleber Z.

, p. 2831 - 2842 (2021/05/13)

Ugi reactions are still a challenge when the concomitant use of ammonia and formaldehyde is required. Herein, we propose a strategy to overcome this challenge using hexamethylenetetramine (HMTA) as a singular key for the employment of these two simple starting materials in the Ugi reaction. Acylaminoacetamide derivatives were prepared in good to excellent yields by this new methodology. The scope and optimization of the reaction conditions were investigated. This novel methodology was successfully applied in the synthesis of two different diketopiperazines (DKPs) using the Ugi/Deprotection+Activation/Cyclization (UDAC) method. A continuous flow approach was also used in this methodology.

Catalyst and solvent-free amidation of inactive esters of N-protected amino acids

Nadimpally, Krishna Chaitanya,Thalluri, Kishore,Palakurthy, Nani Babu,Saha, Abhijit,Mandal, Bhubaneswar

, p. 2579 - 2582 (2011/06/21)

A catalyst free procedure for the preparation of amides from inactive esters of N-protected amino acids and various amines is demonstrated under mild reaction conditions. Our effort to recover excess amine and generated alcohol is an approach towards environment friendly and cost effective synthesis under easy operational conditions.

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