127919-73-7 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
1H-Pyrazole-3-carboxylic acid, 4-(4-fluorophenyl)-, ethyl ester is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, due to its ability to form heterocyclic compounds.
Used in Organic Chemistry:
1H-Pyrazole-3-carboxylic acid, 4-(4-fluorophenyl)-, ethyl ester is used as a reagent in organic chemistry for the preparation of a variety of heterocyclic compounds.
Used in Biomedical and Pharmaceutical Research:
1H-Pyrazole-3-carboxylic acid, 4-(4-fluorophenyl)-, ethyl ester is used as a subject of investigation for its potential antitumor and antimicrobial activities, making it of interest to researchers in the biomedical and pharmaceutical industries.
Used in Materials Science:
1H-Pyrazole-3-carboxylic acid, 4-(4-fluorophenyl)-, ethyl ester may have applications in the field of materials science, although specific uses are not detailed in the provided materials.
Used as a Precursor in Dyes and Pigments Synthesis:
1H-Pyrazole-3-carboxylic acid, 4-(4-fluorophenyl)-, ethyl ester may also have applications as a precursor in the synthesis of dyes and pigments, although the specific applications are not detailed in the provided materials.
Check Digit Verification of cas no
The CAS Registry Mumber 127919-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,1 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 127919-73:
(8*1)+(7*2)+(6*7)+(5*9)+(4*1)+(3*9)+(2*7)+(1*3)=157
157 % 10 = 7
So 127919-73-7 is a valid CAS Registry Number.
127919-73-7Relevant academic research and scientific papers
Nair, Deepa,Pavashe, Prashant,Namboothiri, Irishi N.N.
, p. 2716 - 2724 (2018)
A convenient method for the synthesis of 3-acylpyrazoles and pyrazole-3-carboxylates using diazosulfone as a reactive 1,3-dipole and a diazomethane equivalent is reported here. Chalcones, arylidenemalonates and other arylidene-1,3-dicarbonyls performed we