946655-79-4 Usage
Uses
Used in the Food Industry:
1-(2-Ethyl-2H-pyrazol-3-yl)-ethanone is used as a flavoring agent for its ability to enhance the taste and aroma of food products, contributing to a more appealing consumer experience.
Used in Cosmetic and Personal Care Products:
In the cosmetic and personal care sector, 1-(2-Ethyl-2H-pyrazol-3-yl)-ethanone serves as a fragrance ingredient, adding pleasant scents to products and improving their sensory appeal.
Used in Pharmaceutical Synthesis:
1-(2-Ethyl-2H-pyrazol-3-yl)-ethanone is utilized as an intermediate in the synthesis of various pharmaceuticals, playing a crucial role in the development of new medications.
Used in Agrochemicals:
1-(2-ETHYL-2H-PYRAZOL-3-YL)-ETHANONE also finds application in the agrochemical industry, where it is used as an intermediate in the production of various agrochemicals to support agricultural processes.
Used in Antifungal and Antitumor Research:
1-(2-Ethyl-2H-pyrazol-3-yl)-ethanone has been studied for its potential antifungal and antitumor activities, indicating its possible use in medical and health-related applications.
Check Digit Verification of cas no
The CAS Registry Mumber 946655-79-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,6,6,5 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 946655-79:
(8*9)+(7*4)+(6*6)+(5*6)+(4*5)+(3*5)+(2*7)+(1*9)=224
224 % 10 = 4
So 946655-79-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O/c1-3-9-7(6(2)10)4-5-8-9/h4-5H,3H2,1-2H3
946655-79-4Relevant academic research and scientific papers
An efficient synthesis of isomeric 1-(1-Alkyl-1H-pyrazolyl) ethanones
Taydakov, Ilya,Krasnoselskiy, Sergey
, p. 1422 - 1424 (2013/02/23)
A simple and versatile general method for the preparation of N-substituted 3-, 4-, or 5-acetylpyrazoles from corresponding acids via hydrolysis and decarboxylation of substituted diethyl [(1-alkyl-1H-pyrazolyl)carbonyl]malonates was developed. Title compounds were prepared in three steps without isolation of intermediates in 48-82% overall yield.
