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2-Butenyl 2-(2,4-dichlorophenoxy)acetate

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Identification
Molecular formula
C12H12Cl2O3
CAS number
1929-73-3
IUPAC name
but-2-enyl 2-(2,4-dichlorophenoxy)acetate
State
State

This compound is in a liquid state at room temperature.

Melting point (Celsius)
-9.00
Melting point (Kelvin)
264.15
Boiling point (Celsius)
328.00
Boiling point (Kelvin)
601.15
General information
Molecular weight
295.13g/mol
Molar mass
295.1250g/mol
Density
1.3276g/cm3
Appearence

2-Butenyl 2-(2,4-dichlorophenoxy)acetate is a colorless liquid with a chemical structure that incorporates both chlorophenoxy groups and a butenyl ester group. The combination of these groups contributes to its chemical behavior and physical appearance.

Comment on solubility

Solubility of but-2-enyl 2-(2,4-dichlorophenoxy)acetate

but-2-enyl 2-(2,4-dichlorophenoxy)acetate, a compound often utilized in various chemical applications, exhibits fascinating solubility characteristics. Its behavior in solvents can be summarized as follows:

  • Polar Solvents: This compound generally has limited solubility in polar solvents such as water due to its hydrophobic aromatic structure.
  • Non-Polar Solvents: It shows a better affinity for non-polar or slightly polar solvents such as hexane and ethyl acetate, thanks to its alkene and ester functional groups.
  • Environmental Factors: Temperature may significantly influence solubility; typically, an increase in temperature enhances solubility in non-polar solvents.
  • Dichloro-substitution: The presence of the dichlorophenoxy group influences the solubility, making it less soluble in highly polar environments but soluble in organic solvents.

In conclusion, but-2-enyl 2-(2,4-dichlorophenoxy)acetate demonstrates selective solubility, favoring organic solvents while showing considerable resistance to dissolution in water. The interaction of various functional groups within the compound plays a pivotal role in determining its solubility profile.

Interesting facts

Interesting Facts about But-2-enyl 2-(2,4-dichlorophenoxy)acetate

But-2-enyl 2-(2,4-dichlorophenoxy)acetate is a fascinating chemical compound with various applications and interesting properties. Here are some key insights:

  • Structural Features: This compound belongs to the category of esters, characterized by the presence of an ester functional group. The integration of a 2,4-dichlorophenoxy substituent is particularly notable, as it imparts unique chemical properties.
  • Agricultural Relevance: Due to its structural characteristics, but-2-enyl 2-(2,4-dichlorophenoxy)acetate is often investigated for use in agriculture as a herbicide. Its specific targeting capabilities make it an essential compound for controlling unwanted vegetation while minimizing impact on desired crops.
  • Reaction Pathways: The synthesis of this compound typically involves various organic reaction mechanisms, including nucleophilic substitution and elimination reactions. Understanding these pathways can provide valuable insights for chemists focusing on organic synthesis.
  • Environmental Impact: As with many chemical compounds used in agriculture, the environmental impact of but-2-enyl 2-(2,4-dichlorophenoxy)acetate is an ongoing area of study. Investigating its degradation and accumulation in ecosystems is crucial for ensuring sustainable agricultural practices.
  • Research Potential: This compound demonstrates potential for extensive research, particularly in the development of new, more effective agrochemicals. Its unique structure allows chemists to explore possible modifications that could enhance its efficacy or reduce toxicity.

In summary, but-2-enyl 2-(2,4-dichlorophenoxy)acetate is more than just a chemical; it serves as a bridge between organic chemistry and practical applications in agriculture, highlighting the importance of understanding chemical compounds in addressing real-world challenges.