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Fluorosulfonylchlorfluoroacetylfluoride, also known as compound 2, is a highly reactive and toxic chemical compound with the molecular formula C2ClF3O2S. It is a colorless liquid at room temperature and is known for its strong electrophilic properties. fluorosulfonylchlorfluoroacetylfluoride is primarily used as a reagent in organic synthesis, particularly in the preparation of various fluorinated compounds. Due to its high reactivity, it poses significant health and environmental risks, and therefore, it must be handled with extreme caution and proper safety measures.

2561-79-7

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2561-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2561-79-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2561-79:
(6*2)+(5*5)+(4*6)+(3*1)+(2*7)+(1*9)=87
87 % 10 = 7
So 2561-79-7 is a valid CAS Registry Number.

2561-79-7Upstream product

2561-79-7Downstream Products

2561-79-7Relevant academic research and scientific papers

Ueber die Reaktion von Chlortrifluorethen mit Schwefeltrioxid

Gille, E.,Hass, D.,Holfter, H.,Schoenherr, M.

, p. 145 - 150 (2007/10/02)

Chlorotrifluorethane β-sultone has been synthesized in good yield by bubbling chlorotrifluorethene (CTFE) through liquid sulfur trioxide at atmospheric pressure.By treatment of the sultone with catalytic amounts of triethylamine, quantitative rearrangement to four different fluoroacetylsulfuric acid halides, i.e.F(O)C-CF2-SO2F, F(O)C-CFCl-SO2F, F(O)C-CF2-SO2Cl and F(O)C-CFCl-SO2Cl, occurred.These products were partially separated by fractional distillation.Their concentrations were established from determinations of hydrolyzable halogen and 19F nuclear magnetic resonance spectra.These results confirm that the reaction of CTFE with sulfur trioxide gives approximately equal amounts of the two possible isomeric sultones: which rearrange to fluorodihaloacetylsulfonic acid halides by cyclic mechanism, followed by an F(-)/Cl(-) exchange at the sulfonyl halide groups. - Keywords: Chlorofluorethene; Reaction; Sulfur trioxide; β-Sultone formation; NMR spectroscopy

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