Fluorocyclohexane

Last updated
Fluorocyclohexane
Fluorocyclohexane.svg
Names
Preferred IUPAC name
Fluorocyclohexane
Other names
Cyclohexyl fluoride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.006.141 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 206-754-9
PubChem CID
  • InChI=1S/C6H11F/c7-6-4-2-1-3-5-6/h6H,1-5H2
    Key: GOBGVVAHHOUMDK-UHFFFAOYSA-N
  • C1CCC(CC1)F
Properties
C6H11F
Molar mass 102.152 g·mol−1
AppearanceColorless liquid
Density 0.9280 g/mL
Melting point 13 °C (55 °F; 286 K)
Boiling point 103 °C (217 °F; 376 K)
Insoluble
Hazards
GHS labelling:
GHS-pictogram-flamme.svg GHS-pictogram-exclam.svg
Danger
Flash point 5 °C (41 °F; 278 K)
Related compounds
Related compounds
Chlorocyclohexane
Bromocyclohexane
Iodocyclohexane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Fluorocyclohexane is a organofluorine compound with the chemical formula (CH2)5CHF. [1] [2] [3]

Contents

Synthesis

Fluorocyclohexane is prepared by reaction of cyclohexanol with hydrogen fluoride. [4]

Safety

The compound causes serious skin and eye irritation, and may also cause respiratory irritation. [1]

See also

Related Research Articles

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References

  1. 1 2 "Fluorocyclohexane, 97%, Thermo Scientific Chemicals, Quantity: 5 g | Fisher Scientific". Fisher Scientific . Retrieved 21 June 2023.
  2. "Fluorocyclohexane 372-46-3 | TCI AMERICA". TCI Chemicals. Retrieved 21 June 2023.
  3. Dictionary of Organic Compounds. CRC Press. 1996. p. 3180. ISBN   978-0-412-54090-5 . Retrieved 21 June 2023.
  4. Olah, George A.; Watkins, Michael (1978). "Fluorinations with Pyridinium Polyhydrogen Fluoride Reagent: 1-Fluoroadamantane". Organic Syntheses. 58: 75. doi:10.15227/orgsyn.058.0075.