2340-84-3 Usage
Uses
Used in Surfactant Industry:
1H,1H,2H,3H-PERFLUOROUNDEC-2-EN-1-OL is used as a surfactant for its ability to reduce surface tension, which is beneficial in various industrial processes that require improved wetting, emulsification, and dispersion.
Used in Specialty Chemicals Production:
In the specialty chemicals industry, 1H,1H,2H,3H-PERFLUOROUNDEC-2-EN-1-OL serves as a building block for the synthesis of other fluorinated compounds, leveraging its unique chemical properties to create novel products with specific applications.
Used in Non-stick Coatings:
1H,1H,2H,3H-PERFLUOROUNDEC-2-EN-1-OL is used as a component in non-stick coatings due to its high hydrophobicity and lipophobicity, making it ideal for applications where resistance to water and oil is required, such as in cookware and medical devices.
Used in Other Industrial Applications:
Beyond the mentioned uses, 1H,1H,2H,3H-PERFLUOROUNDEC-2-EN-1-OL finds utility in a variety of other industrial applications, capitalizing on its thermal stability and chemical resistance for performance in demanding environments.
Check Digit Verification of cas no
The CAS Registry Mumber 2340-84-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,4 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2340-84:
(6*2)+(5*3)+(4*4)+(3*0)+(2*8)+(1*4)=63
63 % 10 = 3
So 2340-84-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H5F17O/c12-4(13,2-1-3-29)5(14,15)6(16,17)7(18,19)8(20,21)9(22,23)10(24,25)11(26,27)28/h1-2,29H,3H2/b2-1+
2340-84-3Relevant academic research and scientific papers
Ultrasound-Promoted Selective Perfluoroalkylation on the Desired Position of Organic Molecules
Kitazume, Tomoya,Ishikawa, Nobuo
, p. 5186 - 5191 (2007/10/02)
Perfluoroalkylzinc iodides or bromides wich were prepared from perfluoroalkyl iodides or bromides and zinc powder in N,N-dimethylformamide or tetrahydrofuran with ultrasonic irradiation were found to behave as potential perfluoroalkylating reagents for the preparation of a wide variety of perfluoroalkylated compounds.Especially, the ultrasound-promoted asymmetric induction with perfluoroalkyl group on the asymmetrical carbon was achieved by the reaction of perfluoroalkyl halides with optically active enamines in the presence of zinc powder and a catalytic amount of dichlorobis(?-cyclopentadienyl)titanium.
