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4(1H)-Pyrimidinone, 5-(1,1-dimethylethoxy)-6-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62022-11-1

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62022-11-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62022-11-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,2 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62022-11:
(7*6)+(6*2)+(5*0)+(4*2)+(3*2)+(2*1)+(1*1)=71
71 % 10 = 1
So 62022-11-1 is a valid CAS Registry Number.

62022-11-1SDS

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 6-methyl-5-[(2-methylpropan-2-yl)oxy]-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 5-tert-Butoxy-6-methyl-4-pyrimidon

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:62022-11-1 SDS

62022-11-1Downstream Products

62022-11-1Relevant academic research and scientific papers

Interplay of method development and mechanistic studies - From aerobic oxidative coupling to radical reactions via alkenyl peroxides

Klussmann, Martin,Schweitzer-Chaput, Bertrand

, p. 190 - 202 (2016/01/20)

This account summarizes how scientific advances were made in the authors' research group by combining method development in organic synthesis with detailed mechanistic studies. The discovery of an unexpected autoxidative coupling reaction led, by virtue of an ever increased understanding of its mechanism, to a strategy for green C-H functionalization reactions, novel modes of radical generation, addition reactions of ketones to alkenes and new insights into an old reaction, the Baeyer-Villiger oxidation. 1 Introduction 2 Aerobic Oxidative Coupling Reactions with Benzylic C-H Bonds 2.1 The Autoxidative Coupling with Xanthene 2.2 With a Little Help from Light - CHIPS 2.3 Related Autoxidative Coupling Reactions 3 How Does the Autoxidative Coupling Work? 3.1 An Excursion: Formation of Alkenyl Peroxides from Criegee Intermediates in the Atmosphere 3.2 How do Alkenyl Peroxides Form in Solution? Meet Criegee Again 3.3 The Full Mechanism of the Autoxidative Coupling Reaction 4 Previous Indications for Solution Chemistry of Alkenyl Peroxides 4.1 What Might Alkenyl Peroxides be Good for? 5 Concluding Remarks.

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