354-69-8 Usage
Description
1-IODO-2,2,3,3,3-PENTAFLUOROPROPANE is a halogenated hydrocarbon compound that consists of a propane molecule with one iodine atom and five fluorine atoms attached to it. It is a colorless liquid with a high boiling point and is known for its chemical stability and reactivity.
Uses
Used in Organic Synthesis:
1-IODO-2,2,3,3,3-PENTAFLUOROPROPANE is used as a reagent and intermediate in organic synthesis for the production of various fluorinated compounds. Its unique structure allows for selective reactions and the formation of a wide range of chemical products.
Used in Pharmaceutical Industry:
1-IODO-2,2,3,3,3-PENTAFLUOROPROPANE is used as a building block in the synthesis of pharmaceutical compounds. Its presence in the molecular structure can enhance the drug's properties, such as solubility, stability, and bioavailability, leading to improved therapeutic effects.
Used in Agrochemical Industry:
1-IODO-2,2,3,3,3-PENTAFLUOROPROPANE is used as a precursor in the development of agrochemicals, such as insecticides and herbicides. Its fluorinated nature can contribute to the increased effectiveness and selectivity of these chemicals in controlling pests and weeds.
Used in Production of 1,1,1,2,2-Pentafluoro-Propane:
1-IODO-2,2,3,3,3-PENTAFLUOROPROPANE is used as a raw material to produce 1,1,1,2,2-pentafluoro-propane by heating. 1-IODO-2,2,3,3,3-PENTAFLUOROPROPANE has various applications in different industries, such as refrigerants, foam blowing agents, and as a cleaning solvent.
Check Digit Verification of cas no
The CAS Registry Mumber 354-69-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 354-69:
(5*3)+(4*5)+(3*4)+(2*6)+(1*9)=68
68 % 10 = 8
So 354-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H2F5I/c4-2(5,1-9)3(6,7)8/h1H2
354-69-8Relevant articles and documents
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.
1-Iodo-polyfluoroalkanes from polyfluoroalkoxy trimethylsilanes and iodochloro triphenylphosphorane
Montanari,Quici,Resnati
, p. 1941 - 1944 (2007/10/02)
Polyfluoroalkoxy trimethylsilanes R(f)CH2OSi(CH3)3 (from the alcohols R(f)CH2OH and HMDS), react with Pb3PICI (from ICI and Ph3P) eliminating (CH3)3SiCl. Pyrolysis of the residues gives Ph3PO and pure iodides R(f)CH2I.
