559-54-6 Usage
Uses
Used in Solvent Applications:
2,2,3,3,4,4,4-heptafluoro-1,1-diphenylbutan-1-ol is used as a solvent in various chemical processes due to its high thermal and chemical stability, which allows it to function effectively in harsh conditions.
Used in Surfactant Production:
In the chemical industry, 2,2,3,3,4,4,4-heptafluoro-1,1-diphenylbutan-1-ol is used as a key component in the manufacturing of surfactants. Its unique properties contribute to the performance and stability of the final products.
Used in Polymer Synthesis:
This fluorinated alcohol is also utilized in the production of polymers, where its stability and fluorine content can enhance the polymer's properties, such as resistance to heat and chemicals.
Used in Pharmaceutical Manufacturing:
2,2,3,3,4,4,4-heptafluoro-1,1-diphenylbutan-1-ol finds application in the pharmaceutical industry, where it may be used in the synthesis of various drugs or as a component of drug formulations, leveraging its stability and unique chemical characteristics.
Used in Firefighting Foams:
As a highly effective foam suppressor, 2,2,3,3,4,4,4-heptafluoro-1,1-diphenylbutan-1-ol is used in firefighting foams to control and suppress foam, which is crucial in certain firefighting scenarios to prevent the spread of fire and improve the effectiveness of firefighting efforts.
Used in Other Industries:
2,2,3,3,4,4,4-heptafluoro-1,1-diphenylbutan-1-ol's versatility extends to other industries where its stability and effectiveness in controlling foam are beneficial, such as in industrial processes that require precise foam management.
Check Digit Verification of cas no
The CAS Registry Mumber 559-54-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 559-54:
(5*5)+(4*5)+(3*9)+(2*5)+(1*4)=86
86 % 10 = 6
So 559-54-6 is a valid CAS Registry Number.
559-54-6Relevant academic research and scientific papers
FLUORO-KETONES IV. SYNTHESIS OF PHENYLPERFLUOROALKYL KETONES - MECHANISM OF REACTION BETWEEN PHENYLLITHIUM AND FLUOROESTERS
Chen, Loomis S.,Chen, Grace. J.,Tamborski, Christ
, p. 117 - 130 (2007/10/02)
Although fluorine containing ketones (RfC(O)Rf and RfC(O)R, Rf = perfluoroalkyl) have been prepared from the reaction between organolithium reagents and perfluoroalkyl esters, the reaction has not found general applicability.Variable yields of ketones and co-production of secondary and tertiary alcohol by-products have in most instances been experienced.We have examined in more detail the factors e.g., temperature, mode of addition and perfluoroalkyl ester structure which influence ketone product and by-products formation.By controlling experimental conditions excellent yields of C6H5C(O)Rf compounds can be attained.A lithium salt of a hemiketal (II) has been isolated and shown to be the active intermediate in the production of the ketone.The stability of the salt and its potential reaction with the solvent dictates the type of reaction products.Low temperature favors stability of the lithium salt of the hemiketal whereby high yields of ketones are produced on hydrolysis.
