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4-(dimethylamino)-1-methylpyrimidin-2(1H)-one is a chemical compound with the molecular formula C7H10N2O. It is a derivative of pyrimidin-2(1H)-one, featuring a dimethylamino group at the 4-position and a methyl group at the 1-position. 4-(dimethylamino)-1-methylpyrimidin-2(1H)-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new drugs. Its structure provides a foundation for further chemical modifications, allowing for the exploration of different therapeutic properties. The compound is also of interest in academic research for understanding the reactivity and properties of pyrimidine-based molecules.

2228-27-5

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2228-27-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2228-27-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2228-27:
(6*2)+(5*2)+(4*2)+(3*8)+(2*2)+(1*7)=65
65 % 10 = 5
So 2228-27-5 is a valid CAS Registry Number.

2228-27-5SDS

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 4-(dimethylamino)-1-methylpyrimidin-2-one

1.2 Other means of identification

Product number -
Other names 4-Dimethylamino-1-methyl-1H-pyrimidin-2-on

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

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More Details:2228-27-5 SDS

2228-27-5Downstream Products

2228-27-5Relevant academic research and scientific papers

Reactions with Dimethyl Carbonate, 5 Methylation of the Pyrimidine Bases of Nucleic Acids

Jansen, Helmut in de Wal,Lissel, Manfred

, p. 863 - 865 (2007/10/02)

The methylation of the pyrimidine bases of nucleic acids by dimethyl carbonate is described compared to dimethyl sulphate.The reaction needs higher temperature, a base and the help of 18-crown-6 and DMF as cosolvent. - Keywords: Dimethyl Carbonate, Methylations, Pyrimidine Bases of Nucleic Acids

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