82822-26-2 Usage
Uses
Used in Chemical Intermediates Industry:
(PERFLUOROHEPTANOYL)ACETONE is used as a chemical intermediate for the production of perfluorinated compounds and fluorinated polymers. Its high thermal stability and chemical inertness make it suitable for this application.
Used in Organic Synthesis:
(PERFLUOROHEPTANOYL)ACETONE is used as a solvent in organic synthesis. Its unique properties allow for efficient reactions and improved product yields.
Used in Industrial Applications:
(PERFLUOROHEPTANOYL)ACETONE is used as a surfactant in various industrial applications. Its low surface energy contributes to improved performance and efficiency in these processes.
However, due to its persistence and bioaccumulation in the environment, the use of (PERFLUOROHEPTANOYL)ACETONE is regulated in many countries to minimize potential risks to human health and the ecosystem.
Check Digit Verification of cas no
The CAS Registry Mumber 82822-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,2 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82822-26:
(7*8)+(6*2)+(5*8)+(4*2)+(3*2)+(2*2)+(1*6)=132
132 % 10 = 2
So 82822-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H5F13O2/c1-3(24)2-4(25)5(11,12)6(13,14)7(15,16)8(17,18)9(19,20)10(21,22)23/h2H2,1H3
82822-26-2Relevant academic research and scientific papers
Popova,Ginak
, p. 489 - 494 (2008)
The reactions of unsymmetrical perfluoroalkyl-substituted β-diketones with guanidine, urea, and thiourea gave the corresponding 2-amino-, 2-hydroxy-, and 2-sulfanyl-6-perfluoroalkyl-4-methylpyrimidines.
Regioselective synthesis of 4-alkyl- and 4-aryl-6-(perfluoroalkyl)salicylic acid derivatives by formal [3+3] cyclocondensation of 1,3-bis(silyloxy)-1,3-butadienes with 3-silyloxy-1-(perfluoroalkyl)prop-2-en-1-ones
Büttner, Stefan,Lubbe, Mathias,Reinke, Helmut,Fischer, Christine,Langer, Peter
, p. 7968 - 7976 (2008/12/20)
4-Alkyl- and 4-aryl-6-(perfluoroalkyl)salicylic acid derivatives were regioselectively prepared by [3+3] cyclization of 1,3-bis(silyl enol ethers) with 3-silyloxy-1-(perfluoroalkyl)prop-2-en-1-ones.
