679-03-8 Usage
Uses
Used in Pharmaceutical Industry:
4,4,5,5,6,6,6-HEPTAFLUOROHEX-2-EN-1-OL is used as a building block for the synthesis of various pharmaceuticals, leveraging its reactivity to create complex and effective drug molecules.
Used in Agrochemical Industry:
In the agrochemical sector, 4,4,5,5,6,6,6-HEPTAFLUOROHEX-2-EN-1-OL is used as a key intermediate for the production of insecticides and herbicides, contributing to the development of agricultural chemicals that protect crops from pests and weeds.
Used in Specialty Chemicals Industry:
4,4,5,5,6,6,6-HEPTAFLUOROHEX-2-EN-1-OL is utilized as a reactive intermediate in the synthesis of specialty chemicals, where its unique properties allow for the creation of tailored chemical products for specific applications.
Used in Fluorochemical and Fluoropolymer Production:
4,4,5,5,6,6,6-HEPTAFLUOROHEX-2-EN-1-OL serves as a crucial component in the manufacturing process of fluorochemicals and fluoropolymers, which are known for their exceptional properties such as heat resistance, chemical resistance, and non-stick surfaces.
Safety Considerations:
Check Digit Verification of cas no
The CAS Registry Mumber 679-03-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,7 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 679-03:
(5*6)+(4*7)+(3*9)+(2*0)+(1*3)=88
88 % 10 = 8
So 679-03-8 is a valid CAS Registry Number.
679-03-8Relevant 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.
ULTRASOUND-PROMOTED HYDRPERFLUOROALKYLATION OF ALKYNES WITH PERFLUOROALKYLZINC IODIDE AND COPPER(I) IODIDE
Kitazume, Tomoya,Ishikawa, Nobuo
, p. 1453 - 1454 (2007/10/02)
The reaction of perfluoroalkyl iodides with terminal alkynes and ultrasonically dispersed zinc in the presence of copper(I) iodide proceeded smoothly to give the corresponding vinyl perfluoroalkylides in good yields.
