84336-22-1 Usage
Description
1H,5H-OCTAFLUOROPENTANAL HYDRATE is a chemical compound with the molecular formula C5F8O. It is a hydrate of 1H,5H-octafluoropentanal, which is a colorless liquid with a pungent odor.
Uses
Used in Fluorinated Material Production:
1H,5H-OCTAFLUOROPENTANAL HYDRATE is used as a precursor in the production of fluorinated materials, which are known for their unique properties such as high thermal stability, chemical resistance, and non-flammability.
Used in Organic Chemical Synthesis:
1H,5H-OCTAFLUOROPENTANAL HYDRATE is used as a reagent in organic chemical synthesis, enabling the creation of a variety of complex organic compounds.
Used in Pharmaceutical Industry:
1H,5H-OCTAFLUOROPENTANAL HYDRATE is used as a solvent and intermediate in the pharmaceutical industry, contributing to the development of new drugs and pharmaceutical formulations.
Used in Agrochemical Industry:
1H,5H-OCTAFLUOROPENTANAL HYDRATE is used as a solvent and intermediate in the agrochemical industry, aiding in the production of pesticides and other agricultural chemicals.
Note: While 1H,5H-OCTAFLUOROPENTANAL HYDRATE has various applications, it is also known to be potentially hazardous to human health and the environment. Therefore, proper precautions should be taken when handling and disposing of this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 84336-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,3 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84336-22:
(7*8)+(6*4)+(5*3)+(4*3)+(3*6)+(2*2)+(1*2)=131
131 % 10 = 1
So 84336-22-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H4F8O2/c6-1(7)3(8,9)5(12,13)4(10,11)2(14)15/h1-2,14-15H
84336-22-1Relevant articles and documents
Chiral sulfinamide/achiral sulfonic acid cocatalyzed enantioselective protonation of enol silanes
Beck, Elizabeth M.,Hyde, Alan M.,Jacobsen, Eric N.
supporting information; experimental part, p. 4260 - 4263 (2011/10/08)
The application of chiral sulfinamides and achiral sulfonic acids as a cocatalyst system for enantioselective protonation reactions is described. Structurally simple, easily accessible sulfinamides were found to induce moderate-to-high ee's in the formation of 2-aryl-substituted cycloalkanones from the corresponding trimethylsilyl enol ethers.
Conformational energies of perfluoroalkanes. 5. Dipole moments of H(CF2)nH and H(CF2)nI
Matsuo, Keizo,Stockmayer, Walter H.
, p. 3307 - 3311 (2007/10/02)
Dielectric and refractive index increments at 25°C are reported for some α,ω-dihydroperfluoroalkanes and α-hydro-ω-iodoperfluoroalkanes in benzene and CCl4. Similar measurements on perfluorocyclohexane and perfluoro-n-hexane are used to deduce effective atomic polarizations for fluorocarbons in solution. The dipole moments obtained lead to a somewhat smaller characteristic ratio for the perfluoroalkane chain than had earlier been estimated by Bates and Stockmayer.
