933-19-7

Basic information

• Product Name: 6-Methyl-1,3,5-triazine-2,4(1H,3H)-dione
• Synonyms: 6-Methyl-1,3,5-triazine-2,4(1H,3H)-dione;6-methyl-1H-1,3,5-triazine-2,4-dione
• CAS NO: 933-19-7
• Molecular Formula: C₄H₅N₃O₂
• Molecular Weight: 127.1014
• Product Categories: Amines, Metabolites & Impurities
• Mol File: 933-19-7.mol
• Article Data: 2

Chemical Properties

• Melting Point: 267-276 °C (decomp)
• Appearance: /
• Density: 1.67±0.1 g/cm3(Predicted)
• Storage Temp.: Refrigerator
• Solubility: DMSO, Methanol
• PKA: 6.35±0.70(Predicted)
• CAS DataBase Reference: 6-Methyl-1,3,5-triazine-2,4(1H,3H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Methyl-1,3,5-triazine-2,4(1H,3H)-dione(933-19-7)
• EPA Substance Registry System: 6-Methyl-1,3,5-triazine-2,4(1H,3H)-dione(933-19-7)

Safety Data

• Hazardous Substances Data: 933-19-7(Hazardous Substances Data)

Usage

Uses

6-Methyl-1,3,5-triazine-2,4(1H,3H)-dione is a metabolite of metsulfuron methyl that has been found in soil.

Upstream product

• 591-38-8 acetylbiuret 
• 75-36-5 acetyl chloride 
• 2597-54-8 ethyl acetylcarbamate 
• 57-13-6 urea 
• 74-88-4 methyl iodide 
• 542-02-9 2-methyl-4,6-diamino-1,3,5-triazine 
• 591-07-1 acetylurea 
• 51-79-6 urethane 
• 108-19-0 BIURET 
• 16352-06-0 6-methyl-5-azacytosine 
• 1973-04-2 2,4-dichloro-6-methyl-1,3,5-triazine 
• 60-35-5 acetamide 
• 102-09-0 bis(phenyl) carbonate 
• 42717-42-0 N-t-butylacetamidine 

Downstream Products

• 54449-89-7 2,4-dioxo-1,2,3,4-tetrahydro-pyrrolo[1,2-a][1,3,5]triazine-7-carboxylic acid ethyl ester 
• 108-80-5 isocyanuric acid 
• 75-25-2 Bromoform 

Relevant articles and documents

Synthesis method of triazinopyrrole formic acid

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.