2719854-89-2 Usage
Chemical class
The compound belongs to the class of isoindoline-1,3-diones.
Fluorinated nature
The presence of perfluoropropan-2-yl and oxy groups in the compound indicates its fluorinated nature.
Potential applications
Due to its fluorinated nature, the compound may be useful as a surfactant or in the preparation of fluorinated polymers.
Biological activities
Isoindoline-1,3-dione derivatives have been studied for their various biological activities, including as anticancer, antiviral, and antimicrobial agents, suggesting potential pharmaceutical applications for 2-((perfluoropropan-2-yl)oxy)isoindoline-1,3-dione.
Industrial, chemical, and pharmaceutical applications
The compound has the potential for a wide range of industrial, chemical, and pharmaceutical applications due to its unique structural features.
Check Digit Verification of cas no
The CAS Registry Mumber 2719854-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,7,1,9,8,5 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2719854-89:
(9*2)+(8*7)+(7*1)+(6*9)+(5*8)+(4*5)+(3*4)+(2*8)+(1*9)=232
232 % 10 = 2
So 2719854-89-2 is a valid CAS Registry Number.
2719854-89-2Relevant articles and documents
Nucleophilic and Radical Heptafluoroisopropoxylation with Redox-Active Reagents
Tong, Chao-Lai,Xu, Xiu-Hua,Qing, Feng-Ling
, p. 22915 - 22924 (2021)
The heptafluoroisopropyl group (CF(CF3)2) is prevalent in pharmaceuticals and agrichemicals. However, heptafluoroisopropoxylated (OCF(CF3)2) compounds remain largely underexplored, presumably due to the lack of efficient access to these compounds. Herein, we disclose the practical and efficient heptafluoroisopropoxylation reactions through the invention of a series of redox-active N-OCF(CF3)2 reagents. These reagents were readily prepared from the oxidative heptafluoroisopropylation of hydroxylamines with AgCF(CF3)2. The substitutions on the nitrogen atom significantly affected the properties and reactivities of N-OCF(CF3)2 reagents. Accordingly, two types of N-OCF(CF3)2 reagents including N-OCF(CF3)2 phthalimide A and N-OCF(CF3)2 benzotriazolium salt O′ were used as OCF(CF3)2 anion and radical precursors, respectively. This protocol enables the direct heptafluoroisopropoxylation of a range of substrates, delivering the corresponding products in moderate to excellent yields.
