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4-amino-N-(2-pyrrolidin-1-yl-ethyl)-benzamide is a chemical compound with the molecular formula C12H18N2O. It is a derivative of benzamide, featuring an amino group at the 4-position and a pyrrolidin-1-yl-ethyl side chain attached to the nitrogen atom. 4-amino-N-(2-pyrrolidin-1-yl-ethyl)-benzamide is known for its potential applications in pharmaceutical research, particularly as a building block for the synthesis of various drug candidates. Its structure allows for the exploration of different chemical modifications, which can lead to the development of new therapeutic agents with improved properties. The compound's specific role in drug design is to provide a scaffold that can be further functionalized to target specific biological receptors or enzymes, making it a valuable component in the creation of novel medications.

51-07-0

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51-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51-07-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51-07:
(4*5)+(3*1)+(2*0)+(1*7)=30
30 % 10 = 0
So 51-07-0 is a valid CAS Registry Number.

51-07-0Relevant academic research and scientific papers

Comparative study of dG affinity vs. DNA methylation modulating properties of side chain derivatives of procainamide: Insight into its DNA hypomethylating effect

Gawade,Chakravarty,Debgupta,Sangtani,Narwade,Gonnade,Puranik,Deobagkar

, p. 5350 - 5358 (2016/02/05)

Procainamide derivatives have been synthesized to investigate the role of side chains in modulating the DNA methylation level in cancer cells and gain insight into its mechanism of action. The synthesized derivatives comprised of flexible (dimethyl), cons

Exploration of secondary and tertiary pharmacophores in unsymmetrical N,N′-diaryl urea inhibitors of soluble epoxide hydrolase

Anandan, Sampath-Kumar,Gless, Richard D.

scheme or table, p. 2740 - 2744 (2010/07/15)

The impact of various secondary and tertiary pharmacophores on in vitro potency of soluble epoxide hydrolase (sEH) inhibitors based on the unsymmetrical urea scaffold 1 is discussed. N,N′-Diaryl urea inhibitors of soluble epoxide hydrolase exhibit subtle variations in inhibitory potency depending on the secondary pharmacophore but tolerate considerable structural variation in the second linker/tertiary pharmacophore fragment.

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