375-14-4 Usage
Uses
Used in Coatings and Adhesives Industry:
3,3,4,4,5,5,5-HEPTAFLUORO-2-PENTANOL is used as a surfactant for improving the performance of coatings and adhesives. Its strong wetting capabilities and low surface tension enhance the spreading and adhesion of these products, leading to better coverage and durability.
Used in Consumer Products:
3,3,4,4,5,5,5-HEPTAFLUORO-2-PENTANOL is used as an ingredient in various consumer products due to its ability to improve the performance and stability of formulations. Its unique properties contribute to the effectiveness and longevity of these products.
Used in Medical Field Drug Delivery Systems:
3,3,4,4,5,5,5-HEPTAFLUORO-2-PENTANOL is used as a component in the development of drug delivery systems. Its properties may contribute to the controlled release of medications, improving the efficacy and safety of drug administration.
Used in Medical Field Medical Devices:
3,3,4,4,5,5,5-HEPTAFLUORO-2-PENTANOL has potential applications in the development of medical devices, where its unique properties can enhance the performance and safety of these devices.
However, due to potential environmental and health concerns, the use and handling of 3,3,4,4,5,5,5-HEPTAFLUORO-2-PENTANOL require strict adherence to safety regulations to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 375-14-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 375-14:
(5*3)+(4*7)+(3*5)+(2*1)+(1*4)=64
64 % 10 = 4
So 375-14-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H5F7O/c1-2(13)3(6,7)4(8,9)5(10,11)12/h2,13H,1H3
375-14-4Relevant academic research and scientific papers
Process for hydroxyalkylation of fluorinated alcohols
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, (2008/06/13)
Mono O-hydroxyalkylated derivatives of 1,1-dihydroperfluorinated or 1H,1-alkylperfluorinated alcohols are prepared by reacting the alcohols with alkylene carbonates at a temperature of at least 60° C. in the presence of a one- or two-part catalyst. The catalyst is a nitrogenous base, optionally in combination with a tetraalkylammonium halide. The O-hydroxyalkylated derivatives are useful non-ionic surfactants and emulsifiable compounds for fire extinguishing systems.
ASYMMETRICAL REDUCTION OF PERFLUOROALKYLATED KETONES, KETOESTERS AND VINYL COMPOUNDS WITH BAKER'S YEAST
Kitazume, Tomoya,Ishikawa, Nobuo
, p. 237 - 238 (2007/10/02)
Reduction of perfluoroalkylated ketones, ketoesters and vinyl compounds with baker's yeast was studied.The ketones and β-ketoesters were asymmetrically reduced to give optically active perfluoroalkylated carbinols and hydroxyesters, while the vinyl compounds were reduced to perfluoroalkylated alkanes.
