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3,3,4,4-tetrafluorobutan-2-ol

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Identification
Molecular formula
C4H6F4O
CAS number
79323-08-1
IUPAC name
3,3,4,4-tetrafluorobutan-2-ol
State
State

At room temperature, 3,3,4,4-tetrafluorobutan-2-ol is a liquid.

Melting point (Celsius)
-95.00
Melting point (Kelvin)
178.15
Boiling point (Celsius)
76.30
Boiling point (Kelvin)
349.45
General information
Molecular weight
146.08g/mol
Molar mass
146.0840g/mol
Density
1.2977g/cm3
Appearence

3,3,4,4-Tetrafluorobutan-2-ol is a colorless liquid that may have a mild odor. It is transparent and can appear as a clear solution when pure.

Comment on solubility

Solubility of 3,3,4,4-Tetrafluorobutan-2-ol

3,3,4,4-Tetrafluorobutan-2-ol, with its unique structure, exhibits notable solubility characteristics. Here are some key points to consider:

  • Polar Nature: The presence of multiple fluorine atoms significantly increases the polarity of the molecule, enhancing its solubility in polar solvents.
  • Hydrogen Bonding: The hydroxyl group (-OH) in its structure allows for hydrogen bonding, which also contributes to better solubility in water.
  • Organic Solvents: It is likely to be soluble in various organic solvents such as ethanol and acetone due to its low molecular weight and polar characteristics.

In summary, the solubility of 3,3,4,4-tetrafluorobutan-2-ol can be classified as relatively high in polar environments while still being compatible with many organic solvents. This dual solubility behavior makes it a versatile compound in both aqueous and organic reactions.

Interesting facts

Interesting Facts about 3,3,4,4-Tetrafluorobutan-2-ol

3,3,4,4-Tetrafluorobutan-2-ol is a fascinating compound that combines both fluorine and hydroxyl functional groups, resulting in unique properties. This compound has garnered attention in recent years for its potential applications in various fields.

Key Characteristics:

  • Fluorine Substitution: The presence of four fluorine atoms significantly alters the physical and chemical properties of the butanol molecule. Fluorinated compounds often exhibit enhanced stability and lower reactivity compared to their non-fluorinated counterparts.
  • Alcohol Functionality: As an alcohol, 3,3,4,4-tetrafluorobutan-2-ol can act as a versatile intermediate in organic synthesis, providing opportunities for further functionalization and manipulation in chemical reactions.
  • Potential Applications: Due to its unique structure, this compound may be useful in fields such as pharmaceuticals, agrochemicals, and materials science, where fluorinated compounds are often sought for their beneficial properties.

The study of such compounds reflects the ongoing interest in fluorine chemistry, which continues to reveal new possibilities in the development of innovative materials and technologies. As chemists explore the applications of 3,3,4,4-tetrafluorobutan-2-ol, they uncover the significance of fluorination in enhancing the functionality of organic molecules, paving the way for the next generation of chemical compounds.

Ultimately, this compound serves as a reminder of the intricate relationships within organic chemistry and the continuous quest for knowledge in manipulating molecular structures. Who knows what new discoveries await in the exciting world of tetrafluorobutanol derivatives?

Synonyms
3,3,4,4-TETRAFLUORO-2-BUTANOL, TECH.
654-487-5
3,3,4,4-tetrafluorobutan-2-ol
17425-25-1
2-BUTANOL, 3,3,4,4-TETRAFLUORO-
3,3,4,4-Tetrafluoro-2-butanol
NSC 86107
2,2,3,3-Tetrafluoro-1-Methylpropanol
BRN 1740894
NSC86107
SCHEMBL5436573
SCHEMBL6592953
2-Butanol,3,4,4-tetrafluoro-
DTXSID00880228
UPMGUZUMWYWMKI-UHFFFAOYSA-N
MFCD00021874
NSC-86107
AKOS006275615
CS-0448401
NS00018821