223683-76-9 Usage
Uses
Used in Organic Synthesis:
2,4-Dibromo-6-methylphenyl trifluoromethyl sulphoxide is used as a reagent in organic synthesis for its strong oxidizing properties, which facilitate various chemical reactions and the formation of new compounds.
Used in Chemical Research:
In the field of chemical research, 2,4-Dibromo-6-methylphenyl trifluoromethyl sulphoxide is utilized as a research compound to explore its reactivity and potential applications in developing new chemical processes and materials.
Used in Pharmaceutical Industry:
2,4-Dibromo-6-methylphenyl trifluoromethyl sulphoxide is used as an intermediate in the synthesis of pharmaceutical compounds, leveraging its oxidizing properties to create novel drug molecules with potential therapeutic applications.
Used in Material Science:
In material science, 2,4-Dibromo-6-methylphenyl trifluoromethyl sulphoxide is employed in the development of new materials with specific properties, such as enhanced stability or reactivity, by incorporating its unique chemical structure into the material composition.
Check Digit Verification of cas no
The CAS Registry Mumber 223683-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,6,8 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 223683-76:
(8*2)+(7*2)+(6*3)+(5*6)+(4*8)+(3*3)+(2*7)+(1*6)=139
139 % 10 = 9
So 223683-76-9 is a valid CAS Registry Number.
223683-76-9Relevant academic research and scientific papers
Aryltrifluoromethylsulfoxides: Sulfinylation of aromatics by triflinate salts in acid medium
Wakselman,Tordeux,Freslon,Saint-Jalmes
, p. 550 - 552 (2007/10/03)
Direct sulfinylation reaction of simple aromatic compounds by triflinate salts in triflic acid led to aryltrifluoromethyl sulfoxides. The para isomer was the major one. The regioselectivity of the reaction was very high when the substituent on the aromatic ring was a halogen atom, a trifluoromethoxy group or an acetanilide function.
