722491-64-7 Usage
Uses
Used in Pharmaceutical Industry:
2,2,3,3,3-PENTAFLUORO-1,1-BIS(4-METHOXYPHENYL) PROPANOL is used as a building block for the synthesis of various pharmaceuticals. Its strong electron-withdrawing properties and the presence of methoxyphenyl groups make it a valuable component in the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 2,2,3,3,3-PENTAFLUORO-1,1-BIS(4-METHOXYPHENYL) PROPANOL is utilized as a key intermediate in the synthesis of agrochemicals. Its unique properties contribute to the creation of effective and targeted pesticides and other agricultural chemicals.
Used in Organic Synthesis:
2,2,3,3,3-PENTAFLUORO-1,1-BIS(4-METHOXYPHENYL) PROPANOL is employed as a reagent in various organic synthesis reactions. Its strong electron-withdrawing nature allows for the formation of new chemical bonds and the modification of existing ones, facilitating the synthesis of complex organic molecules for a variety of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 722491-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,2,4,9 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 722491-64:
(8*7)+(7*2)+(6*2)+(5*4)+(4*9)+(3*1)+(2*6)+(1*4)=157
157 % 10 = 7
So 722491-64-7 is a valid CAS Registry Number.
722491-64-7Relevant academic research and scientific papers
Nucleophilic perfluoroalkylation of imines and carbonyls: Perfluoroalkyl sulfones as efficient perfluoroalkyl-transfer motifs
Prakash, G. K. Surya,Wang, Ying,Mogi, Ryo,Hu, Jinbo,Mathew, Thomas,Olah, George A.
supporting information; experimental part, p. 2932 - 2935 (2010/09/09)
Alkoxide-induced nucleophilic pentafluoroethylation and trifluoromethylation of aldehydes, ketones, and imines using pentafluoroethyl phenyl sulfone (PhSO2CF2CF3, 1) and trifluoromethyl phenyl sulfone (PhSO2CF3, 2), respectively, have been successfully achieved. High diastereoselectivity was observed during the perfluoroalkylation of homochiral sulfinimines to give the corresponding perfluoroalkyl sulfinamides.
