680-14-8 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
2,2,3,3,3-Pentafluoro-propionic acid hydrazide is used as a reagent in the synthesis of pharmaceuticals and agrochemicals for its ability to enhance the properties of these compounds, such as increasing their stability and reactivity.
Used in Specialty Polymer Production:
In the polymer industry, 2,2,3,3,3-Pentafluoro-propionic acid hydrazide is used as a building block for the production of specialty polymers. Its unique properties contribute to the development of polymers with specific characteristics, such as improved thermal stability and chemical resistance.
Used in Chemical Analysis:
2,2,3,3,3-Pentafluoro-propionic acid hydrazide is also employed as a reagent in chemical analysis, where its high reactivity allows for the efficient detection and quantification of various chemical species.
Overall, 2,2,3,3,3-Pentafluoro-propionic acid hydrazide plays a significant role in the chemical industry, contributing to the development of innovative pharmaceuticals, agrochemicals, specialty polymers, and enhancing chemical analysis techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 680-14-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 680-14:
(5*6)+(4*8)+(3*0)+(2*1)+(1*4)=68
68 % 10 = 8
So 680-14-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H3F5N2O/c4-2(5,1(11)10-9)3(6,7)8/h9H2,(H,10,11)
680-14-8Relevant academic research and scientific papers
TRICYCLIC COMPOUNDS AND THEIR USE
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Page/Page column 90; 91, (2020/12/29)
Tricyclic compounds and their use are provided. More specifically, tricyclic compounds, pharmaceutical compositions containing them, methods for preparing them, and their use in therapy are also provided.
FLUOROALKYL-CONTAINING β,β'-TRICARBONYL COMPOUNDS: TAUTOMERISM AND REACTION WITH N-NUCLEOPHILES
Krokhalev, V. M.,Saloutin, V. I.,Romas', A. D.,Ershov, B. A.,Pashkevich, K. I.
, p. 316 - 322 (2007/10/02)
The tautomeric composition of α-polyfluoroacyl derivatives of acetylacetone and malonic ester has been established and it has been shown that with N-nucleophiles (ammonia, 1,2-ethylenediamine, o-phenylenediamine) these compounds undergo 'acid' decomposition with the elimination of the polyfluoroacyl group.With hydrazines, malonic ester derivatives react similarly but acetylacetone derivatives undergo cyclization into pyrazoles.The regiodirectivity of the interaction of fluoroalkyl-containing β,β'-tricarbonyl compounds with N-nucleophiles does not depend on their tautomeric composition and is determined by orbital control.
