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1-Chloro-1,2,2-trifluoro-1,2-dinitroethane

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Identification
Molecular formula
C2HClF3N2O4
CAS number
123456-78-9
IUPAC name
1-chloro-1,2,2-trifluoro-1,2-dinitro-ethane
State
State

At room temperature, 1-chloro-1,2,2-trifluoro-1,2-dinitroethane is a liquid.

Melting point (Celsius)
-72.50
Melting point (Kelvin)
200.65
Boiling point (Celsius)
104.70
Boiling point (Kelvin)
377.85
General information
Molecular weight
189.47g/mol
Molar mass
189.4740g/mol
Density
1.6790g/cm3
Appearence

1-Chloro-1,2,2-trifluoro-1,2-dinitroethane is typically a colorless liquid.

Comment on solubility

Solubility of 1-chloro-1,2,2-trifluoro-1,2-dinitro-ethane

The solubility of 1-chloro-1,2,2-trifluoro-1,2-dinitro-ethane is a complex topic, influenced by its unique chemical structure and the presence of various functional groups. This compound, with its halogen and nitro groups, exhibits some interesting characteristics regarding solubility:

  • Polarity: Due to the electronegative fluorine and chlorine atoms, the molecule is polar, which generally aids in solubility in polar solvents.
  • Hydrophobic Interactions: The trifluoromethyl group may lead to hydrophobic interactions, making it less soluble in water.
  • Solvent Compatibility: It is likely more soluble in organic solvents such as acetone, ethanol, or chloroform, where it can participate in van der Waals and dipole-dipole interactions.

In summary, while 1-chloro-1,2,2-trifluoro-1,2-dinitro-ethane shows promising solubility in polar organic solvents, its solubility in water is expected to be limited due to its overall structure. Understanding the solubility characteristics is essential for applications in various chemical processes.

Interesting facts

Interesting Facts about 1-chloro-1,2,2-trifluoro-1,2-dinitro-ethane

1-chloro-1,2,2-trifluoro-1,2-dinitro-ethane, commonly known as a unique fluorinated compound, belongs to the family of halogenated hydrocarbons. This compound is particularly fascinating for several reasons:

  • Location in Chemistry: It is classified as a dinitro compound, which means it contains two nitro groups (-NO2). This characteristic grants it a notable reactivity profile and serves as a useful building block in synthesizing more complex chemicals.
  • Fluorination Effects: The presence of fluorine atoms in its structure enhances its chemical stability and alters its polarity. Fluorinated compounds are often studied for their unique properties, including improved resistance to heat and chemical degradation.
  • Applications: Due to its structure, this compound can find potential applications in various fields. For instance, it can serve in the development of specialty materials, as well as in pharmaceuticals and agrochemicals.
  • Environmental Impact: The environmental implications of fluorinated compounds like this one are under intense study. They contribute to understanding global warming potential and ozone depletion potential, which are critical considerations in today's chemistry research.
  • Research Importance: Scientists are interested in exploring the reactivities of dinitro compounds, as they are involved in various synthesis pathways that are essential for creating novel pharmaceuticals and materials.

In summary, 1-chloro-1,2,2-trifluoro-1,2-dinitro-ethane showcases the intriguing balance between structure and reactivity within organic chemistry. Its distinct features underscore the importance of fluoro-chemistry and dinitro compounds in advancing myriad scientific endeavors.

Synonyms
1-chloro-1,2,2-trifluoro-1,2-dinitroethane
425-11-6
TL 192
BRN 1712069
1-Chloro-1,2-dinitro-1,2,2-trifluoroethane
ETHANE, 1-CHLORO-1,2-DINITRO-1,2,2-TRIFLUORO-
chlorotrifluoro-1,2-dinitroethane
DTXSID00962533