933-19-7 Usage
Uses
Used in Environmental Studies:
6-Methyl-1,3,5-triazine-2,4(1H,3H)-dione is used as a research subject in environmental studies to understand the degradation process of metsulfuron methyl in soil. This helps in assessing the environmental impact of the herbicide and its metabolites, as well as in developing strategies for reducing pesticide residues in the environment.
Used in Soil Analysis:
6-Methyl-1,3,5-triazine-2,4(1H,3H)-dione is used as a marker compound in soil analysis to monitor the presence and concentration of metsulfuron methyl metabolites. This aids in evaluating the effectiveness of soil remediation techniques and in ensuring the safety of agricultural products grown in treated soils.
Used in Pesticide Formulation Development:
Understanding the properties and behavior of 6-Methyl-1,3,5-triazine-2,4(1H,3H)-dione can contribute to the development of new pesticide formulations with reduced environmental impact. By studying its degradation and metabolism, researchers can design safer and more efficient herbicides that minimize the formation of potentially harmful metabolites.
Check Digit Verification of cas no
The CAS Registry Mumber 933-19-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 933-19:
(5*9)+(4*3)+(3*3)+(2*1)+(1*9)=77
77 % 10 = 7
So 933-19-7 is a valid CAS Registry Number.
933-19-7Relevant academic research and scientific papers
Synthesis method of triazinopyrrole formic acid
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Paragraph 0024-0026; 0030-0032; 0035-0037, (2021/11/10)
The invention discloses a synthesis method of triazinopyrrole formic acid, which comprises the following specific steps: (1) by taking a compound II as a raw material, heating and reacting in concentrated sulfuric acid to obtain an intermediate III; (2) carrying out ring closing reaction on the intermediate III and ethyl bromopyruvate to obtain an intermediate IV; and (3) hydrolyzing the intermediate IV in the presence of hydrochloric acid to obtain a target product, namely the compound I. The synthesis method disclosed by the invention is simple to operate, relatively high in yield and suitable for industrial production, and enriches the obtaining way of the fused ring compound.
Retro-ene reactions in heterocyclic synthesis. V. A novel synthetic method for 1,3,5-triazine-2,4(1H,3H)-diones
Ito, Kunio,Sekiguchi, Chiharu,Miida, Asuka Wakai Hiroyuki,Ihara, Shogo
, p. 1533 - 1535 (2008/09/18)
(Chemical Equation Presented) N-t-Butylamidines 1 on heating with diphenyl carbonate (2) at 150-180° gave the 1,3,5-triazine-2,4(1H,3H)-dione derivatives 5. Acylation of amidines 1 and cyclocondensation of the resulting carbamates 3 gave [1,3,5,7]tetrazocine-2,6-dione derivatives 4, and subsequent retro-ene reaction and ring contraction afforded triazine derivatives 5.
