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5-ethyl-5-(3-oxobutyl)pyrimidine-2,4,6(1H,3H,5H)-trione is a complex organic compound with the molecular formula C10H12N2O4. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring containing four carbon atoms and two nitrogen atoms. The compound features an ethyl group at the 5-position and a 3-oxobutyl group at the same position, which is connected to the pyrimidine ring. The 2,4,6-trione functional group indicates the presence of three carbonyl groups (C=O) at these positions, making it a trione. 5-ethyl-5-(3-oxobutyl)pyrimidine-2,4,6(1H,3H,5H)-trione has potential applications in pharmaceuticals and chemical research due to its unique structure and properties.

5579-49-7

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5579-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5579-49-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5579-49:
(6*5)+(5*5)+(4*7)+(3*9)+(2*4)+(1*9)=127
127 % 10 = 7
So 5579-49-7 is a valid CAS Registry Number.

5579-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ethyl-5-(3-oxobutyl)-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names 3'-Ketobutobarbitone

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:5579-49-7 SDS

5579-49-7Upstream product

5579-49-7Downstream Products

5579-49-7Relevant academic research and scientific papers

Butobarbitone metabolism in man: identification of 3' ketobutobarbitone

Grove,Toseland,Draffan,Clare,Williams

, p. 175 - 178 (1974)

After single 200 mg oral doses of butobarbitone (I) in man, 5.4% was excreted in urine unchanged and 28.2% as the 3' hydroxy metabolite (II) in 6 days. A new metabolite, the ketone (III), was detected in urine following oral administration both of I and of II. Oxidation of the hydroxy to the ketone metabolite was demonstrated in vitro with the 9000g fraction of rat liver. Use was made of selective ion monitoring gas chromatography mass spectrometry methods in metabolite detection.

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