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(2,2,2-trifluoroacetyl) 2,2,2-trifluoroacetate

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Identification
Molecular formula
C4F6O2
CAS number
383-63-1
IUPAC name
(2,2,2-trifluoroacetyl) 2,2,2-trifluoroacetate
State
State

At room temperature, (2,2,2-trifluoroacetyl) 2,2,2-trifluoroacetate is typically in a liquid state. It is highly volatile with a low melting point, leading it to remain liquid over a wide range of typical laboratory temperatures.

Melting point (Celsius)
-80.00
Melting point (Kelvin)
193.15
Boiling point (Celsius)
54.00
Boiling point (Kelvin)
327.15
General information
Molecular weight
210.03g/mol
Molar mass
210.0280g/mol
Density
2.1850g/cm3
Appearence

(2,2,2-trifluoroacetyl) 2,2,2-trifluoroacetate is typically a colorless to pale yellow liquid. It has a distinctive sharp, pungent odor characteristic of many fluorinated compounds. The appearance might slightly vary depending on the level of purity and storage conditions.

Comment on solubility

Solubility of (2,2,2-Trifluoroacetyl) 2,2,2-trifluoroacetate

The solubility of (2,2,2-trifluoroacetyl) 2,2,2-trifluoroacetate can be a fascinating aspect to explore, especially considering its unique fluorinated structure. Understanding its solubility involves examining several key factors:

  • Polarity: The compound's extensive use of fluorine atoms introduces significant polarity, affecting how it interacts with solvents.
  • Solvation Effects: The presence of the trifluoroacetyl group can enhance solubility in polar solvents due to hydrogen bonding interactions.
  • Solvent Dependence: Solubility may vary greatly; it is generally more soluble in polar organic solvents (like acetone or methanol) compared to non-polar solvents.
  • Temperature Influence: Increasing temperature often enhances solubility, allowing for a greater dissolution rate.

In summary, while exploring the solubility of (2,2,2-trifluoroacetyl) 2,2,2-trifluoroacetate, one may find that it is more soluble in polar environments due to its unique fluorinated characteristics. As stated, "Solubility is a reflection of molecular interactions." Thus, analyzing these interactions unveils the intriguing behavior of this compound in various solvents.

Interesting facts

Interesting Facts About (2,2,2-Trifluoroacetyl) 2,2,2-Trifluoroacetate

(2,2,2-Trifluoroacetyl) 2,2,2-trifluoroacetate, often abbreviated as TFAT, is a fascinating compound notable for its unique structure and properties. This compound showcases the significant influence of fluorine atoms on chemical behavior. Here are some engaging insights:

  • Fluorine's Effects: The presence of multiple fluorine atoms contributes to the compound's strong electronegativity, resulting in enhanced reactivity and stability. This characteristic makes TFAT particularly interesting in the realm of medicinal chemistry for potential drug design.
  • Role in Synthesis: TFAT can serve as an important intermediate in organic synthesis. It has been utilized in the development of various pharmaceuticals and agrochemicals, demonstrating its versatility in synthetic applications.
  • Environmental Impact: As an organofluorine compound, TFAT raises certain environmental concerns. Fluorinated compounds can be persistent in the environment, leading to ongoing research into their breakdown and safety over time.
  • Structural Insights: The unique structure of TFAT, with its trifluoroacetyl and acetate functionalities, opens up intriguing pathways for studying stereoelectronic effects and reactivity patterns within organic molecules.
  • Applications in Material Science: Due to its distinctive properties, (2,2,2-trifluoroacetyl) 2,2,2-trifluoroacetate is explored in developing advanced materials, including coatings and polymers that require resistance to solvents and chemicals.

As a chemistry student or enthusiast, exploring compounds like TFAT can lead to a deeper understanding of fluorine chemistry and its applications across various scientific disciplines. The fusion of organic synthesis and material science makes this compound a noteworthy subject of study.

In conclusion, (2,2,2-trifluoroacetyl) 2,2,2-trifluoroacetate epitomizes the remarkable ways in which halogens can manipulate molecular behavior, paving the way for innovation in both research and industry.

Synonyms
TRIFLUOROACETIC ANHYDRIDE
407-25-0
Trifluoroacetic acid anhydride
Bis(trifluoroacetic) anhydride
TFAA
Acetic acid, trifluoro-, anhydride
Perfluoroacetic anhydride
Trifluoroacetyl anhydride
2,2,2-trifluoroacetic anhydride
Hexafluoroacetic anhydride
trifluoro acetic anhydride
Anhydrid kyseliny trifluoroctove
5ENA87IZHT
(2,2,2-trifluoroacetyl) 2,2,2-trifluoroacetate
EINECS 206-982-9
NSC 96965
Trifluoroaceticanhydride
2,2,2-trifluoroacetyl 2,2,2-trifluoroacetate
MFCD00000416
TRIFLUOROACETYL 2,2,2-TRIFLUOROACETATE
BRN 0746197
Anhydrid kyseliny trifluoroctove [Czech]
NSC-96965
DTXSID90861920
EC 206-982-9
Acetic acid, 2,2,2-trifluoro-, 1,1'-anhydride
trifluoracetic anhydride
UNII-5ENA87IZHT
C4F6O3
trifiuoroacetic anhydnde
trifloroacetic anhydride
trifluoroactic anhydride
trifluroacetic anhydride
CF3COOCOCF3
triflouroacetic anhydride
trifluoroacteic anhydride
WLN: FXFFVOVXFFF
SCHEMBL52
trifluoro-acetic anhydride
trifluoroacetic anhyd ride
trifluoroaceticacidanhydride
tri-fluoro acetic anhydride
trifluoroacetic acidanhydride
trifluoroaceticacid anhydride
bis(trifluoroacetic)anhydride
trifloroacetic acid anhydride
trifluoracetic acid anhydride
trifluroacetic acid anhydride
CF3C(O)OC(O)CF3
trifluoroacetic acid-anhydride
(CF3CO)2O
O(COCF3)2
trifluoro acetic acid anhydride
trifluoro-acetic acid anhydride
(CF3 CO)2O
Trifluoroacetic anhydride, 99%
tri fluoro acetic acid anhydride
2.2.2-trifluoroacetic anhydride
QAEDZJGFFMLHHQ-UHFFFAOYSA-
DTXCID90810771
Acetic acid, trifluoro, anhydride
BCP08645
CS-B0891
NSC96965
STL299664
2,2,2-trifluoroacetic acid anhydride
AKOS000121328
2,2,2-trifluoro-acetic acid anhydride
FT16186
BP-11375
LS-12969
DB-004104
DB-049641
NS00006815
T0433
Acetic acid, 2,2,2trifluoro, 1,1'anhydride
EN300-19297
D92342
(2,2,2-Trifluoroacetyl)2,2,2-trifluoroacetate
(2,2,2-trifluoroacetyl)-2,2,2-trifluoroacetate
Q411501
Trifluoroacetic anhydride, purum, >=99.0% (GC)
Trifluoroacetic anhydride, ReagentPlus(R), >=99%
F0001-1151
Trifluoroacetic anhydride, for GC derivatization, >=99.0% (GC)
InChI=1/C4F6O3/c5-3(6,7)1(11)13-2(12)4(8,9)10
206-982-9