1868173-15-2 Usage
Uses
Used in Organic Synthesis:
(4-(trifluoromethyl)phenyl)(2,4,6-trimethoxyphenyl)iodonium 4-methylbenzenesulfonate is used as a reagent in organic synthesis for its ability to facilitate chemical reactions and form new compounds. The presence of the iodonium cation makes it a versatile intermediate for the synthesis of various organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (4-(trifluoromethyl)phenyl)(2,4,6-trimethoxyphenyl)iodonium 4-methylbenzenesulfonate is used as a building block for the development of new drugs. The combination of phenyl and trimethoxyphenyl groups, along with the iodonium cation, may contribute to the creation of novel pharmaceutical compounds with potential therapeutic applications.
Used in Materials Science:
(4-(trifluoromethyl)phenyl)(2,4,6-trimethoxyphenyl)iodonium 4-methylbenzenesulfonate is used as a precursor in the synthesis of fluorinated compounds, which are important in materials science for their unique properties, such as increased stability and reactivity.
Used in Chemical Research:
In the field of chemical research, (4-(trifluoromethyl)phenyl)(2,4,6-trimethoxyphenyl)iodonium 4-methylbenzenesulfonate serves as a valuable compound for studying the properties and reactivity of complex organic molecules. Its unique structure allows researchers to explore new reaction pathways and develop innovative synthetic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 1868173-15-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,6,8,1,7 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1868173-15:
(9*1)+(8*8)+(7*6)+(6*8)+(5*1)+(4*7)+(3*3)+(2*1)+(1*5)=212
212 % 10 = 2
So 1868173-15-2 is a valid CAS Registry Number.
1868173-15-2Relevant academic research and scientific papers
Seidl, Thomas L.,Sundalam, Sunil K.,McCullough, Brennen,Stuart, David R.
, p. 1998 - 2009 (2016)
Diaryliodonium salts have recently attracted significant attention as metal-free-arylation reagents in organic synthesis, and efficient access to these salts is critical for advancement of their use in reaction discovery and development. The trimethoxybenzene-derived auxiliary is a promising component of unsymmetrical variants, yet access remains limited. Here, a one-pot synthesis of aryl(2,4,6-trimethoxyphenyl)iodonium salts from aryl iodides, m-CPBA, p-toluenesulfonic acid, and trimethoxybenzene is described. Optimization of the reaction conditions for this one-pot synthesis was enabled by the method of multivariate analysis. The reaction is fast (85% average), and has broad substrate scope (>25 examples) including elaborate aryl iodides. The utility of these reagents is demonstrated in moderate to high yielding arylation reactions with C-, N-, O-, and S-nucleophiles including the synthesis of a liquid crystal molecule.
