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CAS 679-99-2

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1-Chloro-1,2,2,3,3-pentafluoropropane

Description:
1-Chloro-1,2,2,3,3-pentafluoropropane, with the CAS number 679-99-2, is a halogenated hydrocarbon that belongs to the class of fluorinated alkanes. This compound is characterized by its molecular structure, which includes a chlorine atom and five fluorine atoms attached to a three-carbon propane backbone. It is typically a colorless gas or liquid at room temperature, exhibiting low volatility and high stability due to the presence of strong carbon-fluorine bonds. The compound is non-flammable and has a relatively low toxicity profile, making it suitable for various applications, including as a refrigerant and in the production of specialty chemicals. Its physical properties include a low boiling point and high density compared to non-fluorinated hydrocarbons. Additionally, 1-chloro-1,2,2,3,3-pentafluoropropane is of interest in environmental studies due to its potential impact on ozone depletion and global warming, prompting research into its atmospheric behavior and degradation pathways.
Formula:C3H2ClF5
InChI:InChI=1S/C3H2ClF5/c4-1(5)3(8,9)2(6)7/h1-2H
InChI key:InChIKey=FXSNEEBOGAOVIM-UHFFFAOYSA-N
SMILES:C(C(Cl)F)(C(F)F)(F)F
Synonyms:
  • 3-Chloro-1,1,2,2,3-pentafluoropropane
  • HCFC 235ca
  • Propane, 1-Chloro-1,2,2,3,3-Pentafluoro-
  • R 235ca
  • 1-Chloro-1,2,2,3,3-pentafluoropropane
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Found 1 products.
  • 1-Chloro-1,1,2,2,3-Pentafluoropropane
    Biosynth
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    1-Chloro-1,1,2,2,3-Pentafluoropropane

    Controlled Product
    CAS:
    1-Chloro-1,1,2,2,3-Pentafluoropropane (HFC-245fa) is a fluorocarbon that has an electronegative and anisotropic nature. It is a liquid with a boiling point of -95°C. The chemical shift of the methyl group at 2.6 ppm in the 1H NMR spectrum is indicative of a trifluoromethyl group (-CF3). This compound is also soluble in many organic solvents. In addition to being used as a refrigerant and aerosol propellant, it is also used as a surfactant and optical brightener in plastics. Furthermore, 1-chloro-1,1,2,2,3-pentafluoropropane can react with caprylic acid to form HFC-245ea. This reaction occurs because of the steric effect of the trifluoromethyl group on the
    Formula:C3H2ClF5
    Purity:Min. 95%
    Molecular weight:168.49 g/mol

    Ref: 3D-FC83363

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