25016-15-3 Usage
Uses
Used in Pharmaceutical Industry:
1-(1,5-dimethyl-1H-pyrazol-3-yl)ethanone is used as an intermediate for the synthesis of various drugs. Its versatile chemical structure allows for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(1,5-dimethyl-1H-pyrazol-3-yl)ethanone is used as a building block for the creation of pesticides. Its herbicidal, antifungal, and insecticidal properties make it a valuable component in the development of effective and targeted pest control solutions.
Used as a Reagent in Organic Synthesis:
1-(1,5-dimethyl-1H-pyrazol-3-yl)ethanone also serves as a reagent in organic synthesis, facilitating the production of novel chemical entities. Its unique structure and properties enable the synthesis of a wide range of compounds for various applications.
Used in Academic and Industrial Research:
Due to its diverse applications and the potential for further development, 1-(1,5-dimethyl-1H-pyrazol-3-yl)ethanone is a valuable and important chemical in both academic and industrial research. It continues to be a subject of interest for scientists and researchers looking to explore its potential in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 25016-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,1 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25016-15:
(7*2)+(6*5)+(5*0)+(4*1)+(3*6)+(2*1)+(1*5)=73
73 % 10 = 3
So 25016-15-3 is a valid CAS Registry Number.
25016-15-3Relevant academic research and scientific papers
From a simple pyrazole-derived 1,2-amino alcohol to mono- and multinuclear complexes by tailoring hydrogen bond patterns
Seubert, Christoph K.,Sun, Yu,Lan, Yanhua,Powell, Annie K.,Thiel, Werner R.
experimental part, p. 1768 - 1775 (2011/06/25)
Starting from easily accessible ethyl-5(3)-methylpyrazole-3(5)-carboxylate, 2-[(1,5-dimethyl)pyrazol-3-yl]propan-2-ol (3) can be obtained in good yields in just two steps. The latter compound undergoes coordination to a series of transition metal ions; the resulting complexes were characterized by means of spectroscopy and magnetic measurements.
