887268-36-2 Usage
Uses
Used in Pharmaceutical Industry:
1-Fluoro-4-(1,1,2,2-tetrafluoroethoxy)benzene, 4-Fluorophenyl 1,1,2,2-tetrafluoroethyl ether is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with improved properties, such as enhanced solubility, stability, and bioavailability.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Fluoro-4-(1,1,2,2-tetrafluoroethoxy)benzene, 4-Fluorophenyl 1,1,2,2-tetrafluoroethyl ether serves as a crucial building block for the creation of novel agrochemicals. Its incorporation into these compounds can lead to enhanced pesticidal activity, selectivity, and reduced environmental impact.
Used in Materials Science:
1-Fluoro-4-(1,1,2,2-tetrafluoroethoxy)benzene, 4-Fluorophenyl 1,1,2,2-tetrafluoroethyl ether is utilized as a versatile intermediate in the field of materials science. It contributes to the development of advanced materials with unique properties, such as high thermal stability, chemical resistance, and specific optical or electronic characteristics, which can be applied in various industries, including aerospace, electronics, and automotive.
Check Digit Verification of cas no
The CAS Registry Mumber 887268-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,2,6 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 887268-36:
(8*8)+(7*8)+(6*7)+(5*2)+(4*6)+(3*8)+(2*3)+(1*6)=232
232 % 10 = 2
So 887268-36-2 is a valid CAS Registry Number.
887268-36-2Relevant academic research and scientific papers
Nucleophilic tetrafluoroethylation employing in situ formed organomagnesium reagents
Budinská, Alena,Václavík, Ji?í,Matou?ek, Václav,Beier, Petr
supporting information, p. 5844 - 5847 (2016/11/29)
Tetrafluoroalkyl bromides are metalated with equimolar iPrMgCl·LiCl (Turbo Grignard) to form organomagnesium compounds which are stable at low temperatures and react with various electrophiles (aldehydes, ketones, CO2, cyclic sulfate and sulfamidate, N-sulfonylimines, nitrone, chlorophosphate, nonaflyl azide) to afford novel functionalized tetrafluoroethylene-containing products. Ease of operation, excellent selectivity, high nucleophilicity, and enhanced stability of the reactive species together with a broad substrate scope comprise a highly attractive nucleophilic tetrafluoroethylation protocol affording unique synthetic building blocks.
