115347-68-7 Usage
Description
1H,1H,2H,2H-Heptafluoro-3,3-bis(trifluoromethyl)-1-iodohexane is a fluorinated compound with the chemical formula C7F14I. It is a liquid at room temperature and is known for its strong chemical stability, heat and pressure resistance, and low dielectric constant. However, it is toxic and requires careful handling.
Uses
Used in Chemical Reactions and Industrial Processes:
1H,1H,2H,2H-Heptafluoro-3,3-bis(trifluoromethyl)-1-iodohexane is used as a solvent in various chemical reactions and industrial processes due to its strong chemical stability and resistance to heat and pressure.
Used in Electronic Applications:
The low dielectric constant of 1H,1H,2H,2H-Heptafluoro-3,3-bis(trifluoromethyl)-1-iodohexane makes it useful in electronic applications, where its properties can contribute to improved performance and reliability of electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 115347-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,4 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 115347-68:
(8*1)+(7*1)+(6*5)+(5*3)+(4*4)+(3*7)+(2*6)+(1*8)=117
117 % 10 = 7
So 115347-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H4F13I/c9-4(10,5(11,12)8(19,20)21)3(1-2-22,6(13,14)15)7(16,17)18/h1-2H2
115347-68-7Relevant articles and documents
NUCLEOPHILIC CATALYSIS OF THE ADDITION OF TERTIARY PERFLUOROALKYL BROMIDES TO ALKENES AND ALKYNES
Rozhkov, I. N.,Igumnov, S. M.,Pletnev, S. I.,Chaplina, I. V.
, p. 856 (2007/10/02)
-
SYNTHESIS AND CHEMISTRY OF PERFLUORO-2-IODO-2-METHYL-ALKANES
Probst, A.,Raab, K.,Ulm, K.,Werner, K. von
, p. 223 - 246 (2007/10/02)
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.