678-74-0 Usage
Uses
Used in Organic Synthesis:
1H,1H,5H-OCTAFLUOROPENTYL IODIDE is used as a synthetic intermediate for the development of complex organic molecules and pharmaceutical compounds. Its unique structure allows for selective reactions and functional group transformations, making it a valuable component in the synthesis of new and innovative molecules.
Used in Chemical Research:
In the field of chemical research, 1H,1H,5H-OCTAFLUOROPENTYL IODIDE serves as a model compound for studying the properties and reactivity of halogenated hydrocarbons. Its distinct structure provides insights into the behavior of fluorinated and iodinated compounds, contributing to a deeper understanding of their potential applications and limitations.
Used in Material Science:
1H,1H,5H-OCTAFLUOROPENTYL IODIDE is utilized in the development of new materials with specific properties, such as high thermal stability, chemical resistance, and unique electronic characteristics. Its incorporation into polymers, coatings, and other materials can lead to the creation of advanced materials with a wide range of applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1H,1H,5H-OCTAFLUOROPENTYL IODIDE is used as a key component in the synthesis of novel drug candidates. Its unique structure can be exploited to design and develop new therapeutic agents with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Environmental Applications:
1H,1H,5H-OCTAFLUOROPENTYL IODIDE can be employed in environmental applications, such as the development of new methods for the detection and remediation of pollutants. Its unique chemical properties may enable the creation of innovative sensors and technologies for monitoring and addressing environmental challenges.
Check Digit Verification of cas no
The CAS Registry Mumber 678-74-0 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 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 678-74:
(5*6)+(4*7)+(3*8)+(2*7)+(1*4)=100
100 % 10 = 0
So 678-74-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H3F8I/c6-2(7)4(10,11)5(12,13)3(8,9)1-14/h2H,1H2
678-74-0Relevant academic research and scientific papers
Fluorinated organic azides-their preparation and synthetic applications
Tomaszewska, Joanna,Koroniak-Szejn, Katarzyna,Koroniak, Henryk
, p. 421 - 432 (2017/03/09)
Alkyl azides are widely used in many reactions. Although synthesis of such species is relatively well documented, fluorinated azides, especially with large perfluorinated or highly fluorinated groups, are sometimes tricky to make. The presence of fluorine in reacting molecules, sometimes causes significant changes in the reactivity of reacting species. In this paper we give a short overview of re-examination of currently available methods of synthesis of selected azides with highly fluorinated groups.
Highly stereoselective approach to 3-fluoroalkylated (E)-hex-3-ene-1,5- diyne derivatives via an addition-elimination reaction
Konno, Tsutomu,Kishi, Misato,Ishihara, Takashi,Yamada, Shigeyuki
, p. 144 - 151 (2013/11/19)
Palladium(0)-catalyzed Sonogashira cross-coupling reaction of 2-fluoroalkylated (Z)-2-fluoro-1-iodoethene, which is easily prepared from commercially available polyfluorinated alcohols in facile three steps, with terminal alkynes in DMF at room temperature for 24 h took place stereospecifically to give the corresponding 1-fluoroalkylated (Z)-1-fluorobut-1-en-3-yne derivatives in good to excellent yield. Thus obtained fluoroalkylated 1-fluoroenynes were effectively subjected to addition-elimination reaction with various alkynyllithiums at room temperature, leading to 3-fluoroalkylated hex-3-ene-1,5-diyne derivatives in good to high yields with an excellent E selectivity.
α,α,ω-TRIHYDRO-α-HALOPERFLUOROALKANES
Shilin, S. V.,Florensova, O. N.,Chernov, N. F.,Voronkov, M. G.
, p. 1697 - 1699 (2007/10/02)
A synthesis has been developed for α,α,ω-trihydrohaloperfluoroalkanes, H(CF2CF2)n*CH2X, where X is Cl or Br and n is 1 or 4.It is based on the cleavage of the aromatic sulfonate esters of α,α,ω-trihydroperfluoroalkan-α-ols by alkali metal halides.
