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2,2,3-Trichlorobutane-1,1-diol

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Identification
Molecular formula
C4H7Cl3O2
CAS number
996-34-5
IUPAC name
2,2,3-trichlorobutane-1,1-diol
State
State

At room temperature, 2,2,3-Trichlorobutane-1,1-diol is in a solid state.

Melting point (Celsius)
121.00
Melting point (Kelvin)
394.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
181.46g/mol
Molar mass
181.4570g/mol
Density
1.5800g/cm3
Appearence

2,2,3-Trichlorobutane-1,1-diol is typically found as a solid compound at room temperature. It often appears as a white crystalline solid.

Comment on solubility

Solubility of 2,2,3-Trichlorobutane-1,1-diol

The solubility of 2,2,3-trichlorobutane-1,1-diol can be quite interesting due to its unique chemical structure. This compound, with its three chlorine atoms and hydroxyl groups, exhibits distinct solubility behavior in various solvents. Here are some key points to consider regarding its solubility:

  • Polarity: The presence of hydroxyl (-OH) groups contributes to the polarity of the molecule, enhancing its ability to dissolve in polar solvents, such as water.
  • Hydrogen Bonding: The hydroxyl groups can engage in hydrogen bonding, which can significantly increase solubility in water compared to non-polar solvents.
  • Chlorine Influence: The three chlorine substituents introduce non-polar characteristics, potentially leading to reduced solubility in highly polar solvents.
  • Solvent Compatibility: This compound is more soluble in organic solvents like ethanol and acetone than in oils or hydrocarbons.

In summary, the solubility of 2,2,3-trichlorobutane-1,1-diol is influenced by its molecular structure, where the balance of polar (due to hydroxyl groups) and non-polar (due to chlorinated hydrocarbons) characteristics plays a crucial role. This property is essential in applications where solubility in specific media is required, highlighting the importance of understanding solubility in chemical research and practical usage.

Interesting facts

Interesting Facts about 2,2,3-Trichlorobutane-1,1-diol

2,2,3-Trichlorobutane-1,1-diol is a fascinating compound that brings several intriguing aspects to the field of chemistry. Typically encountered in organic synthesis, this compound is notable for its unique structure and potential applications.

Key Highlights:

  • Dual Functionality: This compound contains both hydroxyl groups (-OH) and chloro substituents, which make it versatile in chemical reactions.
  • Intermediary Importance: It often serves as an important intermediate in the synthesis of various pharmaceuticals and agrochemicals.
  • Chirality: With multiple chiral centers, this compound can exist in different stereoisomeric forms, which can influence its reactivity and biological activity.
  • Environmental Considerations: As chlorinated compounds can raise environmental concerns, studying 2,2,3-trichlorobutane-1,1-diol contributes to understanding the behavior and degradation of chlorine-containing organic matter.

Furthermore, the presence of chlorine atoms can enhance the antimicrobial properties of the compound, suggesting potential applications in disinfectants and preservatives. As stated by many researchers, "The strategic incorporation of chlorine in organic molecules can significantly alter their pharmacological profiles."

In summary, 2,2,3-trichlorobutane-1,1-diol is a compound worth studying, not only for its chemical properties but also for its ecological implications and utility in various fields. This balance of structure and function emphasizes the intricate connections found within organic chemistry.

Synonyms
2,2,3-Trichlorobutane-1,1-diol
BUTYLCHLORAL HYDRATE
76-40-4
2,2,3-TRICHLORO-1,1-BUTANEDIOL
EINECS 200-958-1
90FG67M3EK
1,1-Butanediol, 2,2,3-trichloro-
DTXSID00875573
UNII-90FG67M3EK
SCHEMBL9618897
QVYLNOUOIXTUGA-UHFFFAOYSA-N
DTXCID801013694
AKOS024333505
NS00041053
Q27271320
200-958-1