102780-88-1 Usage
Uses
Used in Organic Synthesis:
DECAFLUORO-2-TRIFLUOROMETHYL-2-IODOPENTANE is used as a reagent in organic synthesis for its ability to facilitate the formation of complex molecules. Its unique properties allow for the creation of new compounds with specific characteristics, making it a valuable tool in the development of novel chemical entities.
Used in Coatings Industry:
In the coatings industry, DECAFLUORO-2-TRIFLUOROMETHYL-2-IODOPENTANE is used as a component in the formulation of high-performance coatings. Its low surface energy and high chemical stability contribute to the development of coatings with enhanced durability, resistance to environmental factors, and improved surface properties.
Used in Lubricants Industry:
DECAFLUORO-2-TRIFLUOROMETHYL-2-IODOPENTANE is used as an additive in lubricants to improve their performance. Its high thermal stability and low surface energy enable the development of lubricants with reduced friction, increased wear resistance, and better performance under extreme conditions.
Used in Surfactants Industry:
In the surfactants industry, DECAFLUORO-2-TRIFLUOROMETHYL-2-IODOPENTANE is used as a building block for the preparation of surfactants with unique properties. Its fluorinated structure allows for the creation of surfactants with high surface activity, making them suitable for use in various applications, such as emulsification, wetting, and foaming.
Used in Environmentally Friendly Applications:
Due to its non-toxic and environmentally friendly nature, DECAFLUORO-2-TRIFLUOROMETHYL-2-IODOPENTANE is used as an alternative to traditional organic compounds in certain applications. Its properties make it suitable for use in industries where reducing environmental impact is a priority, such as in the development of green chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 102780-88-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,8 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102780-88:
(8*1)+(7*0)+(6*2)+(5*7)+(4*8)+(3*0)+(2*8)+(1*8)=111
111 % 10 = 1
So 102780-88-1 is a valid CAS Registry Number.
InChI:InChI=1/C6F13I/c7-2(8,3(9,10)6(17,18)19)1(20,4(11,12)13)5(14,15)16
102780-88-1Relevant academic research and scientific papers
Pletnev, S. I.,Igumnov, S. M.,Zakharova, E. V.,Makarov, K. N.
, p. 557 - 560 (1990)
It is shown for the first time that bromination and iodination of tertiary perfluorocarbanions are reversible.The tendency of tertiary perfluoroalkyl halides to undergo dehalofluorination under the influence of weak bases depends on the structure of the perfluoroalkyl halide, and increases in going from lower to higher halides and from linear to cyclic compounds.
Probst, A.,Raab, K.,Ulm, K.,Werner, K. von
, p. 223 - 246 (1987)
Two novel perfluoro-tert-alkyl iodides CF3(CF2)n+1C(CF3)2I have been obtained from F-alkenes CF3(CF2)n-CF=C(CF3)2 (n = 0 and 1) by formal additions of iodine fluoride; these required substantial alterations of known procedures.The F-tert-alkyl iodides are the most reactive alkyl halides known so far, and they are also very toxic.The following types of reactions have been studied: (a) Nucleophilic attack of anions at the iodine, leading to F-alkenes, (b) elimination of iodine fluoride, caused by metals or metal complexes, (c) pyrolysis, to give very selectively F-isobutene and n-perfluoroalkyl iodides, (d) photolysis, and (e) thermally induced insertions into the carbon-iodine bond.Screening results on the inhalation toxicity of the iodides and of some other fluoro-compounds are also reported.
