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3-(Pentafluorosulfanyl)styrene is a chemical compound with the molecular formula C8H5F5S. It is a derivative of styrene, where one of the hydrogen atoms on the benzene ring is replaced by a pentafluorosulfanyl group (SF5). 3-(pentafluorosulfanyl)styrene is characterized by its unique electronic properties due to the presence of the electronegative fluorine atoms in the pentafluorosulfanyl group, which can influence the reactivity and stability of the molecule. It is an important intermediate in the synthesis of various fluorinated organic compounds and has potential applications in the fields of materials science and pharmaceuticals. The compound is typically synthesized through the reaction of styrene with sulfur pentafluoride (SF6) or other fluorinating agents. Due to its reactivity, it is often used in controlled reactions to introduce fluorine-containing groups into organic molecules, which can enhance their chemical and physical properties.

713-39-3

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713-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 713-39-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 713-39:
(5*7)+(4*1)+(3*3)+(2*3)+(1*9)=63
63 % 10 = 3
So 713-39-3 is a valid CAS Registry Number.

713-39-3Downstream Products

713-39-3Relevant academic research and scientific papers

Synthesis and pKa values of 2-(3- and 4- pentafluorosulfanylphenyl)-2-fluorocyclopropylamines

Schinor, Benjamin,Wibbeling, Birgit,Haufe, Günter

, p. 102 - 109 (2013)

Starting from 3- and 4-pentafluorosulfanylbenzaldehydes, a series of cis- and trans-2-aryl-2-fluorocyclopropylamines bearing an SF5 group in 3- or 4-position of the aryl ring were synthesized in 7 steps via the corresponding cyclopropanecarboxylic acids. While the pKa values of the carboxylic acids are very little depending on the stereochemistry at the cyclopropane ring and the regiochemistry of the SF5-substituents in the aryl ring, the pKa of the corresponding 2-fluorocyclopropylamines is strongly dependent on the stereochemistry at the three-membered ring due to hyperconjugative effects of the CF and the CN bonds. Again, the regiochemistry of SF5 substitution in the phenyl ring has almost no influence.

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