[go: up one dir, main page]

Jump to content

Fluorocyclohexane

From Wikipedia, the free encyclopedia
Fluorocyclohexane
Names
Preferred IUPAC name
Fluorocyclohexane
Other names
Cyclohexyl fluoride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.006.141 Edit this at Wikidata
EC Number
  • 206-754-9
  • 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
Appearance Colorless 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:
GHS02: Flammable GHS07: Exclamation mark
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 an organofluorine compound with the chemical formula (CH2)5CHF.[1][2][3]

Synthesis

[edit]

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

Safety

[edit]

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

See also

[edit]

References

[edit]
  1. ^ a b "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.