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2-Hydroxy-4-oxo-1-propyl-N-(pyridin-4-yl)-1,4-dihydroquinoline-3-carboxamide is a complex organic compound with the molecular formula C18H16N2O4. It is a derivative of quinoline, a heterocyclic compound with a benzene ring fused to a pyridine ring. This specific compound features a hydroxyl group (-OH) at the 2-position, a carbonyl group (C=O) at the 4-position, a propyl chain (-CH2CH2CH3) at the 1-position, and a pyridin-4-yl group (a pyridine ring with a nitrogen atom at the 4-position) attached to the nitrogen atom of the quinoline ring. The molecule also contains a carboxamide group (-CO-NH2) at the 3-position. 2-hydroxy-4-oxo-1-propyl-N-(pyridin-4-yl)-1,4-dihydroquinoline-3-carboxamide is of interest in medicinal chemistry due to its potential biological activities and may be involved in the development of new drugs targeting various diseases.

5236-64-6

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5236-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5236-64-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,3 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5236-64:
(6*5)+(5*2)+(4*3)+(3*6)+(2*6)+(1*4)=86
86 % 10 = 6
So 5236-64-6 is a valid CAS Registry Number.

5236-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-4-oxo-1-propyl-N-pyridin-4-yl-quinoline-3-carboxamide

1.2 Other means of identification

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Other names -

1.3 Recommended use of the chemical and restrictions on use

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

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More Details:5236-64-6 SDS

5236-64-6Relevant academic research and scientific papers

SYNTHESIS OF REGIOSPECIFICALLY SUBSTITUTED PYRIMIDYL DERIVATIVES AND THEIR INCORPORATION INTO PENEMS

Capraro, Hans-Georg,Lang, Marc,Schneider, Peter

, p. 643 - 652 (2007/10/02)

Syntheses of regiospecifically substituted pyrimidines are described.Depending on the reaction conditions, N1- or N3-substituted pyrimidines are obtained.It has been shown that substitution on uracil under Mitsunobu conditions yields N1-substituted products.Incorporation of these derivatives into the penem nucleus gives penem antibiotics with extremely long half-lives.

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