Chloride substituents modify the physical properties of organic compounds in several ways. 349-88-2, formula is C6H4ClFO2S, Name is 4-Fluorobenzene-1-sulfonyl chloride. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. COA of Formula: C6H4ClFO2S.
Chen, Xi;Wang, Qiang;Zhang, Zhe;Niu, Zhi-Jie;Shi, Wei-Yu;Gong, Xiao-Ping;Jiao, Rui-Qiang;Gao, Ming-Hui;Liu, Xue-Yuan;Liang, Yong-Min research published 《 Copper-Catalyzed Hydrogen Atom Transfer and Aryl Migration Strategy for the Arylalkylation of Activated Alkenes》, the research content is summarized as follows. Herein, the copper-catalyzed arylalkylation of activated alkenes, e.g., N-(benzenesulfonyl)-N-(4-methoxyphenyl)-2-methylprop-2-enamide via hydrogen-atom transfer and aryl migration strategy were described. The reaction was carried out through a radical-mediated continuous migration pathway using N-fluorosulfonamides, e.g., N-fluoro-4-methyl-N-octylbenzene-1-sulfonamide as the alkyl source. The primary, secondary, and tertiary alkyl radicals formed by intramol. hydrogen-atom transfer proceeded smoothly. This methodol. is an efficient approach for the synthesis of various amide derivatives possessing a quaternary carbon center, e.g., I with good yields and high regioselectivity.
349-88-2, 4-Fluorobenzenesulfonyl chloride is a useful research compound. Its molecular formula is C6H4ClFO2S and its molecular weight is 194.61 g/mol. The purity is usually 95%.
4-Fluorobenzenesulfonyl Chloride is found to be an excellent activating agent for the covalent attachment of biological substances to a variety of solid supports e.g. Sepharose beads. 4-Fluorobenzenesulfonyl Chloride is also used as a reagent for the studies of proteins by fluorine NMR.
4-Fluorobenzenesulfonyl chloride is a reactive chemical that has been shown to have a low safety profile in humans. It is used in the synthesis of replication inhibitors, which are potential anticancer drugs. It also has been shown to inhibit tumor metastasis and growth in mice by binding to the active site of DNA polymerase and inhibiting DNA replication. 4-Fluorobenzenesulfonyl chloride is stable in human liver cells and has been shown to be an effective macroinitiator for proton-coupled electron transfer reactions. This compound has been shown to induce locomotor activity and energy efficiency in rats, which may be due to its ability to increase the number of mitochondria per cell., COA of Formula: C6H4ClFO2S
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics