2993-24-0 Usage
Description
4-AMINOPHENYLSULFUR PENTAFLUORIDE is a light yellow to red-yellow solid that serves as a valuable research chemical with various applications across different industries.
Uses
Used in Research and Development:
4-AMINOPHENYLSULFUR PENTAFLUORIDE is used as a research chemical for its unique properties and potential applications in various scientific fields. It is particularly valuable for studying its chemical behavior and interactions with other compounds, which can lead to the development of new materials and technologies.
Used in Chemical Synthesis:
In the chemical industry, 4-AMINOPHENYLSULFUR PENTAFLUORIDE is used as a reagent or intermediate in the synthesis of various compounds. Its unique structure allows it to participate in specific chemical reactions, contributing to the creation of new molecules with desired properties.
Used in Analytical Chemistry:
4-AMINOPHENYLSULFUR PENTAFLUORIDE can be employed as a reference material or standard in analytical chemistry. Its distinct characteristics make it suitable for calibrating instruments and validating analytical methods, ensuring accurate and reliable results in chemical analysis.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-AMINOPHENYLSULFUR PENTAFLUORIDE is used as a starting material or a building block for the development of new drugs. Its unique chemical properties can be exploited to design and synthesize novel therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Material Science:
4-AMINOPHENYLSULFUR PENTAFLUORIDE can be utilized in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. Its incorporation into material formulations can lead to the creation of advanced materials with applications in various industries, including electronics, energy, and environmental protection.
Check Digit Verification of cas no
The CAS Registry Mumber 2993-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,9 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2993-24:
(6*2)+(5*9)+(4*9)+(3*3)+(2*2)+(1*4)=110
110 % 10 = 0
So 2993-24-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H6F5NS/c7-13(8,9,10,11)6-3-1-5(12)2-4-6/h1-4H,12H2
2993-24-0Relevant articles and documents
Pd-catalyzed direct arylation of nitro(pentafluorosulfanyl)benzenes with aryl bromides
Wang, Chao,Yu, Yan-Bo,Fan, Shilu,Zhang, Xingang
, p. 5004 - 5007 (2013)
Limited methods for the synthesis of SF5-substituted compounds significantly restrict their widespread application. A Pd-catalyzed direct arylation of nitro(pentafluorosulfanyl)benzenes with aryl bromides is reported. This protocol provides a facile and straightforward access to diversified SF5-containing aryl derivatives. The notable features of this reaction are its synthetic simplicity, high reaction efficiency, and good regioselectivity.
Preparation of (Pentafluorosulfanyl)benzenes by Direct Fluorination of Diaryldisulfides: Synthetic Approach and Mechanistic Aspects
Ajenjo, Javier,Klepetá?ová, Blanka,Greenhall, Martin,Bím, Daniel,Culka, Martin,Rulí?ek, Lubomír,Beier, Petr
supporting information, p. 11375 - 11382 (2019/08/20)
Direct fluorination of ortho-, meta- and para-substituted aromatic thiols and disulfides using elemental fluorine afforded substituted (pentafluorosulfanyl)benzenes. This work thus represents the first study of the scope and limitation of direct fluorination for the synthesis of new SF5-containing building blocks. Fluorinations in batch and flow modes were compared. A comprehensive computational study was carried out employing density functional and wave function methods to elucidate the reaction mechanism of the transformation of ArSF3 into ArSF5. Eliminating various nonradical pathways, it has been shown that the reaction proceeds by a radical mechanism, initiated by the attack of the F. on the ArSF3 moiety, propagated via an almost barrierless F2+ArSF4 .→ArSF5+F. step and terminated by the ArSF4 .+F.→ArSF5. Most of the calculated data are in very good agreement with experimental observations concerning the ortho-substituent effect on the reaction rates and yields.
PENTAFLUOROSULPHOLANE-CONTAINING ANTIDIABETIC COMPOUNDS
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Page/Page column 49-50, (2010/08/08)
This invention provides for certain pentafluorosulpholane-containing compounds of the formula or a pharmaceutically acceptable salt, ester, solvate or prodrug thereof, wherein the variables are defined herein; the inventive compounds are agonists of the G