1947-95-1 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2,4-Dichlorophenyl trifluoromethyl sulphoxide is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals for its strong oxidizing properties, which facilitate the production of various compounds.
Used in Organic Synthesis:
2,4-Dichlorophenyl trifluoromethyl sulphoxide is used as a mild and selective oxidizing agent in organic synthesis, enabling the formation of desired products with minimal side reactions.
Used in Crop Protection:
2,4-Dichlorophenyl trifluoromethyl sulphoxide is studied for its potential as a crop protection agent due to its ability to induce resistance to pathogens in plants, enhancing their defense mechanisms against diseases.
Safety Precautions:
It is important to handle 2,4-Dichlorophenyl trifluoromethyl sulphoxide with care, as it can be harmful if ingested or inhaled, and may cause irritation to the skin and eyes. Proper safety measures should be taken during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 1947-95-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,4 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1947-95:
(6*1)+(5*9)+(4*4)+(3*7)+(2*9)+(1*5)=111
111 % 10 = 1
So 1947-95-1 is a valid CAS Registry Number.
1947-95-1Relevant academic research and scientific papers
Method for condensation of aromatic derivative(s) and a sulphinic derivative
-
, (2008/06/13)
The invention concerns a method for the condensation of aromatic derivative(s) or a sulphinic derivative by a perhalogenated, advantageously perfluorinated, carbon atom. Said method is characterized in that it consists in subjecting said sulphinic derivat
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.
