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4,4-dichlorohexan-3-one

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Identification
Molecular formula
C6H10Cl2O
CAS number
7652-92-2
IUPAC name
4,4-dichlorohexan-3-one
State
State

The compound is a liquid at room temperature, making it suitable for use in various organic synthesis applications.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
182.00
Boiling point (Kelvin)
455.15
General information
Molecular weight
155.04g/mol
Molar mass
155.0380g/mol
Density
1.1480g/cm3
Appearence

4,4-Dichlorohexan-3-one is typically a colorless liquid. It may have a sharp, pungent odor that is characteristic of chlorinated ketones.

Comment on solubility

Solubility of 4,4-dichlorohexan-3-one

4,4-dichlorohexan-3-one presents an interesting case in the study of solubility due to its unique chemical structure. This compound has both hydrophobic and hydrophilic characteristics, which influence its solubility in various solvents.

  • Solubility in water: The presence of carbonyl (C=O) groups can lead to some level of solubility in polar solvents like water. However, given that 4,4-dichlorohexan-3-one is relatively bulky due to its hexane backbone and the presence of two chlorine atoms, its overall solubility in water is expected to be limited.
  • Solubility in organic solvents: This compound is likely to be more soluble in organic solvents. Compounds such as acetone, ethanol, or other non-polar to moderately polar solvents can dissolve 4,4-dichlorohexan-3-one effectively because of similar molecular characteristics.

To summarize, the solubility profile of 4,4-dichlorohexan-3-one can be characterized as follows:

  1. Limited solubility in water due to its hydrophobic nature.
  2. Enhanced solubility in organic solvents, making it suitable for various chemical applications.

Understanding the solubility of such compounds is crucial for their application in synthesis and other chemical processes.

Interesting facts

Interesting Facts About 4,4-Dichlorohexan-3-one

4,4-Dichlorohexan-3-one is a notable compound in organic chemistry, primarily due to its unique structure and versatile applications. Here are some fascinating aspects of this compound:

  • Structural Significance: The compound features a ketone functional group that plays a crucial role in its reactivity. The presence of two chlorine atoms enhances its electrophilic nature, which can be exploited in various chemical reactions.
  • Reactivity and Synthesis: This compound can serve as an intermediate in organic synthesis. Its reactive sites make it useful in the formation of more complex molecules, enabling the development of novel chemical entities.
  • Biological Relevance: Compounds with halogen substituents, like 4,4-dichlorohexan-3-one, have garnered attention in pharmaceuticals. The chlorine atoms can influence the biological activity, making them targets for drug design.
  • Environmental Considerations: Given its chlorinated structure, there are safety concerns and environmental impacts associated with 4,4-dichlorohexan-3-one. Halogenated compounds can persist in the environment, necessitating careful handling and disposal.
  • Research Potential: Ongoing research seeks to explore the compound’s potential in various fields, including material science and medicinal chemistry. Its synthesis from simpler starting materials also makes it an attractive candidate for teaching organic synthesis techniques.

In summary, 4,4-dichlorohexan-3-one is not just a compound to study but also a gateway to understanding broader concepts in chemistry. As chemists, we continuously seek to unravel the complexities behind such compounds, pushing the boundaries of what can be achieved through organic synthesis and reactivity.

Synonyms
4,4-DICHLORO-3-HEXANONE
2648-60-4
3-Hexanone, 4,4-dichloro
dichloro-diethyl ethane ether
DTXSID30181073
ZQBGKIGYOVBXJP-UHFFFAOYSA-N