198348-94-6 Usage
General Description
1-ACETYL-5(3)-PHENYL-3(5)-(TRIFLUOROMETHYL)PYRAZOLE is a chemical compound with a pyrazole ring substituted with an acetyl group at the 1-position, a phenyl group at the 5(3)-position, and a trifluoromethyl group at the 3(5)-position. It is a heterocyclic compound that is commonly used in organic synthesis and medicinal chemistry. The trifluoromethyl group enhances the chemical and biological properties of the molecule, making it valuable in drug discovery and development. Additionally, the presence of the phenyl group allows for easy functionalization, further expanding the compound's potential applications. Overall, 1-ACETYL-5(3)-PHENYL-3(5)-(TRIFLUOROMETHYL)PYRAZOLE is a versatile chemical with important implications in various scientific and industrial fields.
Check Digit Verification of cas no
The CAS Registry Mumber 198348-94-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,3,4 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 198348-94:
(8*1)+(7*9)+(6*8)+(5*3)+(4*4)+(3*8)+(2*9)+(1*4)=196
196 % 10 = 6
So 198348-94-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H9F3N2O/c1-8(18)17-11(12(13,14)15)7-10(16-17)9-5-3-2-4-6-9/h2-7H,1H3
198348-94-6Relevant articles and documents
Application of Fe3O4@SiO2@sulfamic acid magnetic nanoparticles as recyclable heterogeneous catalyst for the synthesis of imine and pyrazole derivatives in aqueous medium
Zakerinasab,Nasseri,Hassani,Samieadel
, p. 3169 - 3181 (2016/04/05)
Sulfamic acid supported on Fe3O4@SiO2 superpara magnetic nanoparticles was successfully applied as a recyclable solid acid catalyst with a large density of sulfamic acid groups for the synthesis of pyrazole derivatives, an important class of potentially bioactive compounds. The products are obtained in high yield from the one-pot reaction procedure involving dicarbonyl compounds and hydrazines/hydrazides. This new method totally avoids the use of toxic or expensive solvents and organic acids in this reaction.
Nitropyrazoles: 10. N-nitration of 3(5)-substituted pyrazoles
Dalinger,Litosh,Shevelev
, p. 1149 - 1153 (2007/10/03)
A number of substituted N-nitropyrazoles were prepared by direct nitration of substituted pyrazoles. The dependence of the direction of nitration on the reaction conditions was studied.
