73606-15-2 | 2-[(8-Chloro-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-hexadecafluorooctyl)oxy]-1,1,2,2-tetrafluoroethanesulfonyl fluoride

CAS:73606-15-2 | 2-[(8-Chloro-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-hexadecafluorooctyl)oxy]-1,1,2,2-tetrafluoroethanesulfonyl fluoride ,Description

2-[(8-Chloro-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-hexadecafluorooctyl)oxy]-1,1,2,2-tetrafluoroethanesulfonyl fluoride is a useful research compound. Its molecular formula is C10ClF21O3S and its molecular weight is 634.59 g/mol. The purity is usually 95%.
The exact mass of the compound 2-[(8-Chloro-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-hexadecafluorooctyl)oxy]-1,1,2,2-tetrafluoroethanesulfonyl fluoride is unknown and the complexity rating of the compound is unknown. The storage condition is unknown. Please store according to label instructions upon receipt of goods.Use and application categories indicated by third-party sources: PFAS (per- and polyfluoroalkyl substances) -> OECD Category. However, this does not mean our product can be used or applied in the same or a similar way. 
 

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Scientific Research Applications

Synthesis and Chemical Properties

• Novel Synthesis Methods: New methods have been developed for synthesizing related compounds, such as 1,1,2,2-tetrafluoro-2-(trifluoroethenyloxy)-ethanesulfonyl fluoride, utilizing imidazole protective groups for novel intermediate monomer formation (Uematsu, Hoshi, & Ikeda, 2006).
• Functional Monomer and Copolymerization: Studies on the synthesis of functional monomers and their copolymerization with tetrafluoroethylene, using related fluorosulfonyl compounds, have been reported (Kostov, Kotov, Ivanov, & Todorova, 1993).

Environmental and Industrial Applications

• PFOS Alternatives in Sewage Sludge: Research identified novel polyfluorinated ether sulfonates, similar to the given compound, as alternatives to perfluorooctanesulfonate (PFOS) in the electroplating industry, especially in municipal sewage sludge in China (Ruan et al., 2015).
• Redox Treatability in Chrome Mist Suppressant Solutions: The role of hydrogenated moiety in the redox treatability of fluorotelomer sulfonic acid, used as an alternative to PFOS and PFOA in chrome mist suppressants, has been studied, indicating effective treatment methodologies (Bao et al., 2020).

Chemical Reactions and Interactions

• Deoxyfluorination Applications: Research on the deoxyfluorination of peracetylated pyranose hemiacetals with related fluoroalkanesulfonyl fluoride compounds has been conducted, highlighting its potential in glycosyl fluoride synthesis (Yan, Lai, Tian, & Yu, 2012).
• Noncovalent Interactions Analysis: Studies have focused on contrasting the noncovalent interactions of aromatic sulfonyl fluoride motifs, providing insights into their structural and property correlations (Bellia et al., 2022).

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