53841-58-0 Usage
Uses
Used in Pharmaceutical Industry:
2-(PENTAFLUOROPROPENYL)ACETATE is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its high reactivity allows for the creation of complex molecules that can be used in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(PENTAFLUOROPROPENYL)ACETATE is utilized as a reactive intermediate in the production of pesticides and other crop protection agents, contributing to the development of effective and safe agricultural chemicals.
Used in Organic Synthesis:
2-(PENTAFLUOROPROPENYL)ACETATE is used as a solvent and a reagent in various organic synthesis processes. Its unique properties facilitate specific chemical reactions, making it an essential component in the synthesis of specialty chemicals and materials.
Used in Fine Chemicals Production:
2-(PENTAFLUOROPROPENYL)ACETATE is also employed in the production of fine chemicals, where its reactivity and stability are crucial for creating high-quality end products with precise molecular structures.
Check Digit Verification of cas no
The CAS Registry Mumber 53841-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,4 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53841-58:
(7*5)+(6*3)+(5*8)+(4*4)+(3*1)+(2*5)+(1*8)=130
130 % 10 = 0
So 53841-58-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H3F5O2/c6-2(1-3(11)12)4(7)5(8,9)10/h1H2,(H,11,12)/b4-2+
53841-58-0Relevant academic research and scientific papers
Polyfluorinated enol acetates
Zeifman, Yu. V.,Postovoi, S. A.,German, L. S.
, p. 170 - 172 (2007/10/02)
The synthesis of polyfluorinated enol acetates has been performed by reductive dechlorination of chloropolyfluoroketones with zinc in Ac2O.Under these conditions, hexafluoroacetone is preferably reduced at the carbonyl group. - Key words: polychlorofluoroketones; reductive dehalogenation; polyfluorinated enol acetates; synthesis; reactivity.
