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3,5-dimethylpyridin-2(1H)-one, also known as 2-acetyl-3,5-dimethylpyridine, is an organic compound with the molecular formula C8H9NO. It is a derivative of pyridin-2(1H)-one, featuring two methyl groups at the 3rd and 5th positions and an acetyl group at the 2nd position. This heterocyclic compound is characterized by its aromatic structure and exhibits various chemical properties, such as reactivity towards nucleophiles and electrophiles. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds due to its versatile chemical structure. The compound is typically synthesized through various methods, including condensation reactions and Friedel-Crafts acylation, and can be further functionalized to access a wide range of derivatives.

3718-67-0

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3718-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3718-67-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,1 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3718-67:
(6*3)+(5*7)+(4*1)+(3*8)+(2*6)+(1*7)=100
100 % 10 = 0
So 3718-67-0 is a valid CAS Registry Number.

3718-67-0SDS

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 3,5-dimethyl-1H-pyridin-2-one

1.2 Other means of identification

Product number -
Other names 3,5-dimethyl-pyridone

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:3718-67-0 SDS

3718-67-0Relevant academic research and scientific papers

Controlled oxygen release from pyridone endoperoxides promotes cell survival under anoxic conditions

Benz, Sebastian,N?tzli, Sarah,Siegel, Jay S.,Eberli, Daniel,Jessen, Henning J.

, p. 10171 - 10182 (2014/01/17)

In tissue engineering, survival of larger constructs remains challenging due to limited supply of oxygen caused by a lack of early vascularization. Controlled release of oxygen from small organic molecules represents a possible strategy to prevent cell death under anoxic conditions. A comprehensive study of methylated pyridone-derived endoperoxides has led to the development of water-soluble molecules that undergo retro-Diels-Alder reactions in aqueous environment releasing oxygen in high yield and with half-lives of up to 13 h. These molecules in combination with vitamin C as singlet oxygen quencher significantly improved survival of 3T3 fibroblasts and rat smooth muscle cells challenged with oxygen-depleted conditions.

OXYGENATION OF THE UNACTIVATED PYRIDINE SYSTEM BY ACETYL HYPOFLUORITE MADE DIRECTLY FROM F2

Rozen, Shlomo,Hebel, David

, p. 249 - 258 (2007/10/02)

Acetyl hypofluorite was found capable of activating the usually unreactive pyridine by substituting the hydrogen at the 2 position by an acetoxy group which then was hydrolyzed to the corresponding pyridinone.Substitutents at 3, 4 or 5 position do not interfere with the reaction, but compounds with substituents at 2 (with the exception of aromatic ones) either do not react or produce tars.The reaction conditions are very mild and the yields are very good for this kind of substitution.Quinolines and pyrazines also react very satisfactorily.

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