1422-41-9 Usage
Structure
A benzene ring with a fluorine atom at the 1st position and a pentafluorothio substituent at the 3rd position
Structure
A benzene ring with a fluorine atom at the 1st position and a pentafluorosulphanyl substituent at the 3rd position
Properties
Highly fluorinated, potentially useful in organic synthesis and pharmaceutical development, valuable for studying the effects of fluorine and sulfur substitution on the reactivity and properties of aromatic compounds
Properties
Highly fluorinated, potentially useful in organic synthesis and pharmaceutical development, valuable for studying the effects of fluorine and sulfur substitution on the reactivity and properties of aromatic compounds, potential applications in the development of new materials or in the design of bioactive molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 1422-41-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1422-41:
(6*1)+(5*4)+(4*2)+(3*2)+(2*4)+(1*1)=49
49 % 10 = 9
So 1422-41-9 is a valid CAS Registry Number.
1422-41-9Relevant academic research and scientific papers
Silver-induced self-immolative Cl-F exchange fluorination of arylsulfur chlorotetrafluorides: Synthesis of arylsulfur pentafluorides
Cui, Benqiang,Jia, Shichong,Tokunaga, Etsuko,Saito, Norimichi,Shibata, Norio
supporting information, p. 12738 - 12741 (2017/12/06)
A novel strategy for the synthesis of arylsulfur pentafluorides by silver carbonate-induced Cl-F exchange fluorination of arylsulfur chlorotetrafluorides is reported. This fluorination does not require any exogenous fluoride sources. Rather, the reaction proceeds via the self-immolation of the substrate Ar-SF4Cl.
INDUSTRIAL METHODS FOR PRODUCING ARYLSULFUR PENTAFLUORIDES
-
Page/Page column 26-27, (2012/09/10)
Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.
