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Benzaldehyde, 4-[(4-cyclopropyl-1-piperazinyl)carbonyl]-, is a complex organic compound with the molecular formula C18H20N2O2. It is a derivative of benzaldehyde, featuring a 4-cyclopropyl-1-piperazinylcarbonyl group attached to the 4-position of the benzene ring. Benzaldehyde, 4-[(4-cyclopropyl-1-piperazinyl)carbonyl]- is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. Its structure allows for the formation of diverse chemical entities, making it a valuable intermediate in medicinal chemistry. The compound's unique properties, such as its ability to form stable bonds and its reactivity, contribute to its utility in creating new therapeutic agents.

929622-21-9

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929622-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 929622-21-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,6,2 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 929622-21:
(8*9)+(7*2)+(6*9)+(5*6)+(4*2)+(3*2)+(2*2)+(1*1)=189
189 % 10 = 9
So 929622-21-9 is a valid CAS Registry Number.

929622-21-9Relevant academic research and scientific papers

Novel benzamide-based histamine H3 receptor antagonists: The identification of two candidates for clinical development

Letavic, Michael A.,Aluisio, Leah,Apodaca, Richard,Bajpai, Manoj,Barbier, Ann J.,Bonneville, Anne,Bonaventure, Pascal,Carruthers, Nicholas I.,Dugovic, Christine,Fraser, Ian C.,Kramer, Michelle L.,Lord, Brian,Lovenberg, Timothy W.,Li, Lilian Y.,Ly, Kiev S.,McAllister, Heather,Mani, Neelakandha S.,Morton, Kirsten L.,Ndifor, Anthony,Nepomuceno, S. Diane,Pandit, Chennagiri R.,Sands, Steven B.,Shah, Chandra R.,Shelton, Jonathan E.,Snook, Sandra S.,Swanson, Devin M.,Xiao, Wei

, p. 450 - 454 (2015/04/27)

The preclinical characterization of novel phenyl(piperazin-1-yl)methanones that are histamine H3 receptor antagonists is described. The compounds described are high affinity histamine H3 antagonists. Optimization of the physical properties of these histamine H3 antagonists led to the discovery of several promising lead compounds, and extensive preclinical profiling aided in the identification of compounds with optimal duration of action for wake promoting activity. This led to the discovery of two development candidates for Phase I and Phase II clinical trials.

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