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Acetic acid 1,2-dihydro-1,6-dimethyl-2-oxopyridin-4-yl ester, also known as 1,6-dimethyl-2-oxo-1,2-dihydropyridine-4-yl acetate, is a chemical compound with the molecular formula C10H13NO3. It is a derivative of acetic acid, where the hydroxyl group is replaced by a 1,6-dimethyl-2-oxo-1,2-dihydropyridine-4-yl group. Acetic acid 1,2-dihydro-1,6-dimethyl-2-oxopyridin-4-yl ester is characterized by its aromatic structure and the presence of a pyridine ring, which contributes to its chemical properties. It is used in various chemical reactions and synthesis processes, particularly in the pharmaceutical and agrochemical industries, due to its potential applications in the development of active ingredients. The compound's structure and reactivity make it a valuable intermediate in the synthesis of more complex molecules.

7211-75-8

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7211-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7211-75-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,1 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7211-75:
(6*7)+(5*2)+(4*1)+(3*1)+(2*7)+(1*5)=78
78 % 10 = 8
So 7211-75-8 is a valid CAS Registry Number.

7211-75-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1,2-dimethyl-6-oxopyridin-4-yl) acetate

1.2 Other means of identification

Product number -
Other names 4-acetoxy-1,6-dimethyl-2-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:7211-75-8 SDS

7211-75-8Relevant academic research and scientific papers

3-acyl-1,2,3,4-tetrahydropyridine-2,4-diones: Synthesis and chemical properties

Rubinov,Zheldakova,Rubinova,Baranovskii

, p. 432 - 439 (2008/12/22)

N-Substituted 6-methyl-1,2,3,4-tetrahydropyridine-2,4-diones reacted with aliphatic carboxylic acid chlorides in the presence of pyridine or triethylamine to give the corresponding 4-O-acyl derivatives which underwent O,C-migration of the acyl group by the action of 2 equiv of triethylamine and a catalytic amount of 2-hydroxy-2-methylpropanenitrile. Reactions of 3-acyl-6-methyl-1,2,3,4- tetrahydropyridine-2,4-diones thus formed with aliphatic and aromatic amines gave the corresponding enamino derivatives at the side acyl group. Enamino derivatives at the C4 =O group were obtained by transformation of 3-acyl-1,2,3,4-tetrahydropyridine-2,4-diones into 3-acyl-4-methoxy-6-methyl-1,2- dihydropyridin-2-ones via alkylation with dimethyl sulfate and subsequent treatment with amines.

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