2728-75-8 Usage
Uses
Used in Organic Synthesis:
E/Z-1-IODO-2-(HEPTAFLUOROPROPYL)CYCLOHEXANE is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the creation of a wide range of organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, E/Z-1-IODO-2-(HEPTAFLUOROPROPYL)CYCLOHEXANE is used as a precursor in the development of new drugs. Its unique structure allows for the exploration of its potential therapeutic properties and incorporation into medicinal compounds.
Used in Agrochemical Research:
E/Z-1-IODO-2-(HEPTAFLUOROPROPYL)CYCLOHEXANE is utilized in agrochemical research as a component in the formulation of crop protection products, potentially enhancing the effectiveness of pesticides and other agricultural chemicals.
Used in the Synthesis of Functional Materials:
The heptafluoropropyl group in E/Z-1-IODO-2-(HEPTAFLUOROPROPYL)CYCLOHEXANE makes it a useful building block for synthesizing functional materials, which can have applications in various industries such as electronics, coatings, and adhesives.
Used in the Production of Specialty Chemicals:
E/Z-1-IODO-2-(HEPTAFLUOROPROPYL)CYCLOHEXANE is also used in the synthesis of specialty chemicals, where its unique properties can be leveraged to create high-value products for specific applications in industries like chemical manufacturing and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 2728-75-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,2 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2728-75:
(6*2)+(5*7)+(4*2)+(3*8)+(2*7)+(1*5)=98
98 % 10 = 8
So 2728-75-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H10F7I/c10-7(11,8(12,13)9(14,15)16)5-3-1-2-4-6(5)17/h5-6H,1-4H2
2728-75-8Relevant academic research and scientific papers
Process for preparing polyfluoroalkyl-substituted compounds
-
, (2008/06/13)
A process for preparing a perfluoroalkyl-substituted compound is disclosed. The process comprises reacting a halopolyfluoroalkane having 1 to 20 carbon atoms with a compound selected from the group consisting of (1) a substituted or unsubstituted ethylene, (2) a substituted or unsubstituted acetylene and (3) a substituted or unsubstituted allylsilane, in the presence of a metal-carbonyl complex of the metal of the Group VIII of the Periodic Table. Alternatively, the reaction between the halopolyfluoroalkane and the substituted or unsubstituted allylsilane is effected under radical generating condition.
New Efficient Palladium-Catalyzed Perfluoroalkylation of Carbon-Carbon Multiple Bonds with F-Alkyl Iodides. An Expedient Route to F-Alkylated Alkyl and Alkenyl Iodides
Ishihara, Takashi,Kuroboshi, Manabu,Okada, Yoshiji
, p. 1895 - 1896 (2007/10/02)
A variety of alkenes and alkynes efficiently undergo the perfluoroalkylation with F-alkyl iodides in the presence of a catalytic amount of tetrakis(triphenylphosphine)palladium(0) in hexane to give good yields of the corresponding F-alkylated alkyl and al
