140647-19-4 Usage
Uses
Used in Research and Development:
3,5-Bis(trifluoromethyl)-1-phenylpyrazole is used as a research chemical for exploring its unique properties and potential applications. Its complex structure, which includes the phenyl and trifluoromethyl groups, may offer insights into new chemical reactions or interactions that could be valuable in various scientific fields.
Used in Chemical Synthesis:
In the chemical industry, 3,5-Bis(trifluoromethyl)-1-phenylpyrazole may serve as an intermediate or a building block in the synthesis of more complex molecules. Its specific structural features could be harnessed to create novel compounds with tailored properties for use in pharmaceuticals, materials science, or other specialized applications.
Used in Material Science:
3,5-Bis(trifluoromethyl)-1-phenylpyrazole could be employed in material science research to investigate its potential as a component in the development of new materials with unique electronic, optical, or mechanical properties. The presence of fluorine atoms in the trifluoromethyl groups may contribute to the compound's stability or reactivity, making it an interesting candidate for further study in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 140647-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,4 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 140647-19:
(8*1)+(7*4)+(6*0)+(5*6)+(4*4)+(3*7)+(2*1)+(1*9)=114
114 % 10 = 4
So 140647-19-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H6F2O2/c1-4(11)6-2-5(9)3-7(10)8(6)12/h2-3,12H,1H3
140647-19-4Relevant articles and documents
Synthesis of fluorinated heterocycles
Sloop, Joseph C.,Bumgardner, Carl L.,Loehle, W. David
, p. 135 - 147 (2007/10/03)
Selected 1,3-diketones having a trifluoromethyl group and/or a fluorine in the 2-position were condensed with aromatic hydrazines, hydroxylamine, urea, thiourea, guanidine, and substituted anilines producing pyrazoles, isoxazoles, pyrimidines, and quinolines, respectively, in yields ranging from 27 to 87%.
