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N-ethyl-3-methoxy-N-[(6-methyl-2-oxo-1,2-dihydroquinolin-3-yl)methyl]benzamide is a complex organic compound with the molecular formula C22H24N2O4. It is a derivative of benzamide, featuring a quinoline ring structure attached to the benzene ring through a methylene bridge. The compound exhibits a methoxy group at the 3rd position of the benzene ring and an ethyl group at the nitrogen atom. This chemical is known for its potential applications in the pharmaceutical industry, particularly as an inhibitor of the enzyme dipeptidyl peptidase-4 (DPP-4), which plays a role in the regulation of glucose levels in the body. The compound's structure allows it to interact with the enzyme, potentially leading to therapeutic benefits for conditions such as type 2 diabetes.

5272-63-9

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5272-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5272-63-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,7 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5272-63:
(6*5)+(5*2)+(4*7)+(3*2)+(2*6)+(1*3)=89
89 % 10 = 9
So 5272-63-9 is a valid CAS Registry Number.

5272-63-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-3-methoxy-N-[(6-methyl-2-oxo-1H-quinolin-3-yl)methyl]benzamide

1.2 Other means of identification

Product number -
Other names HMS2507N24

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5272-63-9 SDS

5272-63-9Downstream Products

5272-63-9Relevant academic research and scientific papers

Imidazo[1,5-a]pyridine-3-ylidenes and dipyridoimidazolinylidenes as ancillary ligands in Palladium allyl complexes with potent in vitro anticancer activity

Andreetta, Giovanni,Canzonieri, Vincenzo,Demitri, Nicola,Mauceri, Matteo,Rizzolio, Flavio,Scattolin, Thomas,Visentin, Fabiano

, (2021)

The synthesis and characterization of silver and palladium allyl complexes bearing imidazo[1,5-a]pyridine-3-ylidene and dipyridoimidazolinylidene ligands is reported. NMR analysis of the starting azolium salts revealed the weaker σ-donor character of these NHC ligands compared to the most common imidazol-2-ylidenes and imidazolin-2-ylidenes. All cationic palladium allyl complexes showed remarkable antitumoral activity toward a panel of cisplatin-sensitive and cisplatin-resistant cell lines, with IC50 in the micro- and nano-molar range. Among the tested derivatives, those with a pyridine arm combine good anticancer activity with a poor cytotoxicity against normal cells. Finally, all palladium complexes, especially the bisNHC species, showed good photoluminescence properties, with emission in the blue/green region.

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