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5,6-DIMETHYL-3,4-DIHYDRO-1H-PYRIDIN-2-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52648-22-3

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52648-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52648-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,4 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52648-22:
(7*5)+(6*2)+(5*6)+(4*4)+(3*8)+(2*2)+(1*2)=123
123 % 10 = 3
So 52648-22-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO/c1-5-3-4-7(9)8-6(5)2/h3-4H2,1-2H3,(H,8,9)

52648-22-3SDS

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 5,6-DIMETHYL-3,4-DIHYDRO-1H-PYRIDIN-2-ONE

1.2 Other means of identification

Product number -
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

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:52648-22-3 SDS

52648-22-3Downstream Products

52648-22-3Relevant academic research and scientific papers

Preparation and Reaction of Pyridones: Steric and Electronic Effects on Cycloadditions with 2(1H)-Pyridones

Gisby, Graham P.,Royall, Sven E.,Sammes, Peter G.

, p. 169 - 174 (2007/10/02)

The reactions of series of substituted 2(1H)-pyridones with dimethyl butynedioate have been studied.Cycloadditions across the 3,6-positions can be observed in certain instances and are particularly favoured where steric buttressing occurs between the substituent groups of the starting pyridones.The pyridone could not be induced to react with simple olefins, either by intermolecular or, via incorporation of alkenyl substituents, by intramolecular processes.From the results it is shown that 2-pyridones can be encouraged to behave as reactive classical dienes in cycloaddition reactions.

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