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1-Chloro-6-fluorohexane

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Identification
Molecular formula
C6H12ClF
CAS number
690-10-8
IUPAC name
1-chloro-6-fluoro-hexane
State
State
It is a liquid at room temperature, which is a typical physical state for many small aliphatic halogenated hydrocarbons.
Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.15
Boiling point (Celsius)
152.00
Boiling point (Kelvin)
425.15
General information
Molecular weight
140.61g/mol
Molar mass
140.6100g/mol
Density
1.0185g/cm3
Appearence

1-Chloro-6-fluorohexane is a clear, colorless liquid. It does not have a distinctive color and appears similar to many other simple organic compounds.

Comment on solubility

Solubility of 1-chloro-6-fluoro-hexane

1-chloro-6-fluoro-hexane, a halogenated hydrocarbon, presents unique solubility characteristics mainly due to its structure and functional groups. Understanding its solubility behaviors can be crucial in various applications.

  • Polar vs. Nonpolar: The presence of both a chlorine atom and a fluorine atom in the molecule suggest a moderate polarity. However, because hexane is predominantly nonpolar, solubility in water is limited.
  • Solvent Compatibility: 1-chloro-6-fluoro-hexane is likely to be soluble in organic solvents such as:
    • Ethyl acetate
    • Hexane
    • Chloroform
  • Temperature Effects: As with many organic compounds, solubility may increase with temperature, leading to greater dissolution in organic solvents.

In summary, while 1-chloro-6-fluoro-hexane is not soluble in water, its compatibility with nonpolar organic solvents makes it a valuable compound in various chemical processes. These solubility factors play a significant role in its applications and reactions in laboratories and industrial settings.

Interesting facts

Exploring 1-Chloro-6-fluoro-hexane

1-Chloro-6-fluoro-hexane is a fascinating organic compound that showcases the complexity and versatility of halogenated alkanes. As a member of the hexane family, its structure contains both chlorine and fluorine atoms, which contribute to its unique properties and reactivity.

Key Characteristics

  • Halogenation: The presence of chlorine and fluorine atoms makes this compound an example of halogenated hydrocarbons, which are widely studied for their roles in organic synthesis and industrial applications.
  • Applications: Due to its functional groups, 1-chloro-6-fluoro-hexane has potential uses in various fields, including pharmaceuticals, agriculture, and as intermediates in chemical manufacturing.
  • Toxicity and Environmental Impact: Like many halogen-containing compounds, careful consideration of toxicity and environmental impact is crucial when handling this substance, especially regarding its persistence in the environment.

Chemical Behavior

The unique regulation of the Cl and F atoms influences the compound's reactivity. For instance, fluorinated hydrocarbons often exhibit enhanced stability and reactivity towards nucleophiles, making them valuable in various chemical reactions.

Scientific Significance

This compound serves as a valuable model for studying the interactions between halogens and hydrocarbons. Understanding these relationships can aid in the development of new materials and improve existing chemical processes.

In conclusion, 1-chloro-6-fluoro-hexane is not only a textbook example of an organic halide but also a compound that exemplifies the cutting-edge interplay between chemistry, application, and environmental considerations in modern science.

Synonyms
1-chloro-6-fluorohexane
1550-09-0
HEXANE, 1-CHLORO-6-FLUORO-
6-Fluorohexyl chloride
BRN 1732406
1-chloro-6-fluoro-hexane
4-01-00-00350 (Beilstein Handbook Reference)
SCHEMBL3444878
DTXSID80165787
AKOS006277107
DB-226208