Skip to main content

1,2,3-Trifluorobenzene

ADVERTISEMENT
Identification
Molecular formula
C6H3F3
CAS number
14190-13-1
IUPAC name
1,2,3-trifluorobenzene
State
State

At room temperature, 1,2,3-Trifluorobenzene is in a liquid state. It is volatile and may evaporate into the air if left exposed.

Melting point (Celsius)
-28.00
Melting point (Kelvin)
245.15
Boiling point (Celsius)
138.20
Boiling point (Kelvin)
411.35
General information
Molecular weight
146.09g/mol
Molar mass
146.1120g/mol
Density
1.3360g/cm3
Appearence

1,2,3-Trifluorobenzene appears as a colorless liquid. It has a distinct aromatic odor and is similar in appearance to other volatile organic compounds.

Comment on solubility

Solubility of 1,2,3-Trifluorobenzene

1,2,3-Trifluorobenzene, with the chemical formula C6H3F3, presents distinctive solubility characteristics due to its trifluoromethyl substituents. Generally, the solubility of organic compounds can be influenced by various factors, including polarity, molecular size, and the nature of surrounding solvents.

Key points regarding its solubility:

  • Polarity: The presence of fluorine atoms makes 1,2,3-trifluorobenzene relatively polar, yet less polar compared to alcohols or carboxylic acids. This affects its solubility in different solvents.
  • Solvent Compatibility: It is known to be soluble in organic solvents like ethanol and acetone, while having limited solubility in water due to its hydrophobic aromatic structure.
  • Influence of Temperature: Like many organic compounds, its solubility can increase with temperature, particularly in non-polar solvents.

In summary, while 1,2,3-trifluorobenzene exhibits solubility in certain organic solvents, its solubility in water is notably low, typical of aromatic compounds with significant fluorination. As always, specific solubility conditions can depend on various environmental and experimental factors.

Interesting facts

Interesting Facts about 1,2,3-Trifluorobenzene

1,2,3-Trifluorobenzene is a fascinating compound that showcases the unique properties and behavior of fluorinated aromatic compounds. Here are some intriguing aspects of this compound:

  • Structural Aspect: 1,2,3-Trifluorobenzene consists of a benzene ring with three fluorine atoms substituted at the 1, 2, and 3 positions. This specific arrangement contributes to its distinct chemical reactivity and physical properties compared to other fluorobenzenes.
  • Fluorination Effects: The introduction of fluorine atoms significantly alters the electron density and polarizability of the benzene ring. As a result, 1,2,3-trifluorobenzene exhibits enhanced reactivity in electrophilic substitution reactions.
  • Applications: This compound is utilized in various applications ranging from the synthesis of functional materials to being a building block in pharmaceuticals and agrochemicals. It plays a role in the development of formulations that require the unique characteristics of fluorinated compounds.
  • Physical Properties: While specific physical properties were not mentioned, fluorinated compounds like 1,2,3-trifluorobenzene often exhibit increased stability and resistance to degradation, making them valuable in harsh chemical environments.

As a chemistry student, one can appreciate the balance of theory and practical application that compounds like 1,2,3-trifluorobenzene represent. The use of fluorine, a highly electronegative element, is a powerful tool in organic chemistry, leading to compounds with tailored properties.

1,2,3-Trifluorobenzene serves as a reminder of how slight modifications in molecular structure can lead to significant changes in chemical behavior. This compound not only represents an interesting study subject but is also a crucial player in advancing various fields of research.

Synonyms
1,2,3-TRIFLUOROBENZENE
Benzene, 1,2,3-trifluoro-
DTXSID90164125
DTXCID2086616
625-446-9
ajknnujqfalrik-uhfffaoysa-n
1489-53-8
trifluorobenzene
MFCD00012013
Benzene, trifluoro-
3,4,5-trifluoro-benzene
C6H3F3
3,4,5-trifluorobenzene
SCHEMBL180426
1,2,3-Trifluorobenzene, >=98%
AKOS006223911
AC-8267
FT104428
PS-10253
DB-042961
CS-0128836
T2356
EN300-160012