15285-15-1 Usage
Uses
Used in Agricultural Industry:
3-Chloro-5-methyl-1,2,4-triazole is used as a preservative in the agricultural industry to protect crops from fungi and bacteria. Its antimicrobial properties help maintain the health and quality of crops, reducing the impact of microbial infections.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 3-Chloro-5-methyl-1,2,4-triazole is used as a key intermediate in the synthesis of various drugs. Its unique chemical structure allows for the development of new compounds with potential therapeutic applications.
Used in Dye Synthesis:
3-Chloro-5-methyl-1,2,4-triazole is also utilized in the synthesis of dyes due to its ability to form stable complexes with other molecules. This property makes it a valuable component in the creation of dyes with specific color characteristics and stability.
Used in Other Organic Compounds Synthesis:
3-CHLORO-5-METHYL-1,2,4-TRIAZOLE's versatility extends to the synthesis of other organic compounds, where it can be used to create a variety of products with different applications across various industries.
It is crucial to handle 3-Chloro-5-methyl-1,2,4-triazole with care, as improper use may lead to toxic effects on human health and the environment. Proper safety measures and regulations should be followed to ensure its safe application in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 15285-15-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,8 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15285-15:
(7*1)+(6*5)+(5*2)+(4*8)+(3*5)+(2*1)+(1*5)=101
101 % 10 = 1
So 15285-15-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H4ClN3/c1-2-5-3(4)7-6-2/h1H3,(H,5,6,7)
15285-15-1Relevant articles and documents
Oxidative Alkylation of Azoles. II. Reactions of 1,3-Dichloro-5-R-1,2,4-triazoles with Methyl Iodide
Kurenkov, A. A.,Pevzner, M. S.,Trubitsin, A. E.
, p. 103 - 109 (2007/10/03)
Reactions of 1,3-dichloro-5-R-1,2,4-triazoles with methyl iodide yield mono- and bicyclic 1,4-dimethylthiazolium salts.In addition, 3-chloro-5-R-1,2,4-triazoles unsubstituted at the nitrogen atoms and N-monomethyl derivatives are formed.