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4-nitro-N-(2-pyrrolidin-1-yl-ethyl)-benzamide is a complex organic chemical compound with the molecular formula C13H18N3O3. It is a derivative of benzamide, featuring a nitro group at the 4-position and a pyrrolidin-1-yl-ethyl side chain attached to the nitrogen atom. 4-nitro-N-(2-pyrrolidin-1-yl-ethyl)-benzamide is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting the central nervous system. Its structure allows for the exploration of various biological activities, such as modulation of neurotransmitter systems, which could be relevant for the treatment of neurological disorders or pain management. The compound's specific properties and potential uses are subjects of ongoing scientific investigation, highlighting the importance of understanding its chemical behavior and interactions within biological systems.

1664-30-8

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1664-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1664-30-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,6 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1664-30:
(6*1)+(5*6)+(4*6)+(3*4)+(2*3)+(1*0)=78
78 % 10 = 8
So 1664-30-8 is a valid CAS Registry Number.

1664-30-8Relevant 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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