16352-06-0 Usage
Description
4-AMINO-6-METHYL-1,3,5-TRIAZIN-2-OL, also known as Acetoguanide, is a degradation product of the sulfonylurea herbicide Iodosulfuron. It is characterized by its off-white solid appearance and is derived from the chemical breakdown of the herbicide.
Uses
Used in Agricultural Industry:
4-AMINO-6-METHYL-1,3,5-TRIAZIN-2-OL is used as a degradation product for [application reason] related to the agricultural industry, specifically in the context of herbicide use and its environmental impact. The application reason could be for understanding the environmental fate of the parent herbicide, Iodosulfuron, or for assessing its potential ecological risks.
Used in Chemical Research:
4-AMINO-6-METHYL-1,3,5-TRIAZIN-2-OL is used as a subject of study in chemical research for [application reason] to explore its properties, reactivity, and potential applications in various chemical processes. The application reason could be to understand its chemical behavior, to develop new synthetic routes, or to identify possible uses in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 16352-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,5 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16352-06:
(7*1)+(6*6)+(5*3)+(4*5)+(3*2)+(2*0)+(1*6)=90
90 % 10 = 0
So 16352-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N4O/c1-2-6-3(5)8-4(9)7-2/h1H3,(H3,5,6,7,8,9)
16352-06-0Relevant articles and documents
Kinetics and Hydrolysis Mechanism of Triasulfuron
Braschi, Ilaria,Calamai, Luca,Cremonini, Mauro Andrea,Fusi, Paolo,Gessa, Carlo,Pantani, Ottorino,Pusino, Alba
, p. 4495 - 4499 (1997)
The hydrolysis of the sulfonylurea herbicide triasulfuron [(2-(2-chloroethoxy)-N-[[4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl] benzenesulfonamide] was studied in aqueous buffers of pH values 2, 3, 4, 5, 6, 7, and 9. The reaction was of first-order and pH-dependent. Triasulfuron was more persistent in neutral or weakly basic than in acidic solution. Five metabolites have been isolated and identified. At all pH values studied, the primary pathway of degradation was the cleavage of the sulfonylurea bridge. However, minor degradation pathways have also been observed like O-demethylation and opening of the triazine ring. The product distribution was pH-dependent.
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Klosa
, p. 139 (1955)
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