52225-57-7 Usage
Uses
Used in Chemical Research:
2,2,2-TRIFLUORO-N-(2,2,2-TRIFLUORO-1-TRIFLUOROMETHYL-ETHYLIDENE)-ACETAMIDE is used as a research compound for studying its reactivity and properties in various chemical reactions. Its unique structure allows scientists to explore its potential applications and interactions with other chemical entities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2,2-TRIFLUORO-N-(2,2,2-TRIFLUORO-1-TRIFLUOROMETHYL-ETHYLIDENE)-ACETAMIDE is used as a building block for the synthesis of fluorinated pharmaceutical compounds. The presence of fluorine atoms can significantly influence the pharmacokinetic and pharmacodynamic properties of drugs, making 2,2,2-TRIFLUORO-N-(2,2,2-TRIFLUORO-1-TRIFLUOROMETHYL-ETHYLIDENE)-ACETAMIDE a valuable asset in the development of novel therapeutic agents.
Used in Agrochemical Industry:
2,2,2-TRIFLUORO-N-(2,2,2-TRIFLUORO-1-TRIFLUOROMETHYL-ETHYLIDENE)-ACETAMIDE is also utilized in the agrochemical industry as a starting material for the synthesis of fluorinated agrochemicals. The incorporation of fluorine atoms can enhance the stability, selectivity, and efficacy of these compounds, leading to improved performance in agricultural applications.
Used in Materials Science:
In the field of materials science, 2,2,2-TRIFLUORO-N-(2,2,2-TRIFLUORO-1-TRIFLUOROMETHYL-ETHYLIDENE)-ACETAMIDE is employed as a component in the development of advanced materials with unique properties. The presence of fluorine atoms can impart specific characteristics, such as increased stability, hydrophobicity, or thermal resistance, making 2,2,2-TRIFLUORO-N-(2,2,2-TRIFLUORO-1-TRIFLUOROMETHYL-ETHYLIDENE)-ACETAMIDE a valuable resource for material innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 52225-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,2 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52225-57:
(7*5)+(6*2)+(5*2)+(4*2)+(3*5)+(2*5)+(1*7)=97
97 % 10 = 7
So 52225-57-7 is a valid CAS Registry Number.
InChI:InChI=1/C5F9NO/c6-3(7,8)1(4(9,10)11)15-2(16)5(12,13)14
52225-57-7Relevant academic research and scientific papers
POLYFLUORINATED 1,3,5-OXADIAZINES
Sinyakov, Yu. V.,Vasil'ev, N. V.,Kolomiets, A. F.,Sokol'skii, G. A.
, p. 578 - 584 (2007/10/02)
The dehydration of polyfluorinated N,N'-diacyl-2,2-diaminopropanes with high-strength oleum gave the previously uninvestigated 2,4,4,6-polyfluoroalkyl-substituted 1,3,5-oxadiazines.It also proved possible to obtain these compounds in the reaction of 4,4,6-tris(trifluoromethyl)-1,3,2,5-dioxathiazine-2,2-dione with amides.A characteristic feature of the chemical properties of the polyfluorinated 1,3,5-oxadiazines is their susceptibility to anionotropic transformations.Here nucleophilic attack on the C=N bond results in ring opening, which is regiospecific in the case of hard bases and regiononselsctive with 1-butanethiol.
Amide and fluoroxy derivatives of N-perfluoroacylhexafluoroisopropylidenimines
Peterman, Keith E.,Shreeve, Jean'ne M.
, p. 2705 - 2709 (2008/10/08)
LiN=C(CF3)2 readily undergoes metathetical reactions with perfluoroacyl halides to give perfluoroacylimines. The new acylimines, RfC(O)N=C(CF3)2 (Rf = CF3, C2F5), are susceptible to polar addition of XY (XY = HF, HCl, ClF) across the C=N bond to yield the corresponding secondary and tertiary amides, RfC(O)NXCY(CF3)2. Direct fluorination of CF3C(O)N=C(CF3), under catalytic conditions produces a fluoroamide, CF3C(O)NFCF(CF3)2, from saturation of the C=N function and a fluoroxy compound CF3CF(OF)NFCF(CF3)2 from further addition across the C=O bond.
