107432-46-2 Usage
Uses
Used in Pharmaceutical Industry:
HEPTAFLUORO-1-(1,2,2,2-TETRAFLUORO-1-IODOETHOXY)PROPANE is used as an intermediate compound for the synthesis of iodine-containing perfluoro compounds. These perfluoro compounds have potential applications in the pharmaceutical industry, such as in the development of contrast agents for medical imaging, drug delivery systems, and as components in the synthesis of other bioactive molecules.
Used in Chemical Synthesis:
In the field of chemical synthesis, HEPTAFLUORO-1-(1,2,2,2-TETRAFLUORO-1-IODOETHOXY)PROPANE serves as a valuable precursor for the preparation of various perfluoroalkyl-containing compounds. Its unique structure allows for further functionalization and the creation of new molecules with tailored properties for specific applications.
Used in Material Science:
HEPTAFLUORO-1-(1,2,2,2-TETRAFLUORO-1-IODOETHOXY)PROPANE is used as a building block in the development of novel materials with specific properties, such as high thermal stability, chemical resistance, and low surface energy. These materials can be utilized in various industries, including aerospace, electronics, and coatings.
Used in Environmental Applications:
Due to its perfluorinated nature, HEPTAFLUORO-1-(1,2,2,2-TETRAFLUORO-1-IODOETHOXY)PROPANE can be employed in the development of environmentally friendly alternatives to traditional perfluorinated compounds, which have raised concerns due to their persistence and potential toxicity. HEPTAFLUORO-1-(1,2,2,2-TETRAFLUORO-1-IODOETHOXY)PROPANE can be used to create safer and more sustainable materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 107432-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,3 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107432-46:
(8*1)+(7*0)+(6*7)+(5*4)+(4*3)+(3*2)+(2*4)+(1*6)=102
102 % 10 = 2
So 107432-46-2 is a valid CAS Registry Number.
InChI:InChI=1/C5F11IO/c6-1(7,2(8,9)10)4(14,15)18-5(16,17)3(11,12)13
107432-46-2Relevant articles and documents
Synthesis of new nitrogen-containing perfluoroalkyl iodides
Fukaya, Haruhiko,Hayashi, Eiji,Hayakawa, Yoshio,Abe, Takashi
, p. 117 - 123 (1997)
Perfluoro(dimethylamino)-, perfluoro(diethylamino)-, perfluoro(1-pyrrolidinyl)-, perfluoromorpholino-, perfluoropiperidino-and perfluoropropoxy-substituted perfluoroalkyl iodides were synthesized directly by the reaction of the corresponding perfluoroacyl fluorides with lithium iodide in high yield. Under controlled reaction conditions, it was possible to synthesize either iodo-perfluoroacyl fluorides or perfluoroalkylidene diiodides by the reaction of perfluoro(alkanedioyl) difluorides with lithium iodide. Perfluoro(α-alkylamino-substituted alkyl) iodides may be good candidates for the media of solar-pumped lasers.
CHEMISTRY OF POLYFLUOROCARBONS. 1. NUCLEOPHILIC IODOFLUORINATION OF PERFLUOROALKYL VINYL ETHERS
Nazarenko, T. I.,Deev, L. E.,Ponomarev, V. G.,Novosel'tseva, N. I.,Pospelova, N. B.,Pashkevich, K. I.
, p. 586 - 588 (2007/10/02)
Nucleophilic iodofluorination of perfluorovinyl methyl (I) and perfluorovinyl propyl (II) ethers by iodine chloride in nitrobenzene or sulfolan afforded 1-iodoperfluoro-1-methoxyethane (III) and 1-iodoperfluoro-1-propoxyethane in yields of 65 and 77percent, respectively.In addition to compound (III), the reaction of perfluorovinyl methyl ether afforded two side products: 1-iodo-2-chloroperfluoro-1-methoxyethane and 2-iodo-1-chloroperfluoro-1-methoxyethane.The latter products are formed via a radical reaction, which takes place under drastic conditions.On the basis of quantum chemical calculations of (I), (II), and the two anions formed from (I),CF3OC-FCF3 (VI) and CF3OCF2C-F2 (VII), it is proposedd that nucleophilic iodofluorination of perfluoroalkyl vinyl ethers involves the formation of thermodinamically more stable anions.The higher reactivity of (I) compared with (II) is in accord with the energy of the lowest unoccupied molecular orbitals and the charge density on the CF2 carbon atoms. 19F NMR spectra of the synthesized products are shown.
