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3-Chlorobut-2-enylbenzene

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Identification
Molecular formula
C10H11Cl
CAS number
2516-47-8
IUPAC name
3-chlorobut-2-enylbenzene
State
State

3-Chlorobut-2-enylbenzene is usually found in a liquid state at room temperature. It is not highly volatile and remains stable under normal conditions.

Melting point (Celsius)
-52.00
Melting point (Kelvin)
221.15
Boiling point (Celsius)
239.00
Boiling point (Kelvin)
512.15
General information
Molecular weight
168.65g/mol
Molar mass
168.6460g/mol
Density
0.9964g/cm3
Appearence

3-Chlorobut-2-enylbenzene is a colorless to pale yellow liquid. It may appear transparent and has a low viscosity. Due to its chemical structure, it might release an aromatic odor.

Comment on solubility

Solubility of 3-chlorobut-2-enylbenzene

3-chlorobut-2-enylbenzene, also known as an allylbenzene with a chlorine substituent, offers intriguing solubility characteristics that can be influenced by various factors:

  • Polar vs. Nonpolar Solvents: This compound's structure includes a chlorinated segment, which tends to enhance its solubility in polar solvents due to the chlorine atom's electronegativity. However, the benzene ring and the aliphatic chain also contribute to its affinity for nonpolar solvents.
  • Temperature Effects: As with many organic compounds, elevated temperatures can lead to increased solubility as molecular motion enhances solvent interactions.
  • Concentration Considerations: In dilute solutions, 3-chlorobut-2-enylbenzene is likely to exhibit better solubility compared to saturated solutions, where solubility limits might be reached.

In summary, the solubility of 3-chlorobut-2-enylbenzene is moderate and is largely dependent on the solvent used, temperature, and concentration. As a result, it may show good behavior in organic solvents while demonstrating limited solubility in water. The molecular structure plays a critical role in determining its solubility properties and limits, creating a fascinating area for further exploration in chemical studies.

Interesting facts

Interesting Facts about 3-chlorobut-2-enylbenzene

3-chlorobut-2-enylbenzene, also known as a derivative of styrene, presents a fascinating intersection of aromatic and aliphatic chemistry. This compound features both a benzene ring and an alkenyl side chain, making it particularly interesting for various chemical reactions and applications. Here are some engaging insights:

  • Structural Diversity: The dual nature of 3-chlorobut-2-enylbenzene, which incorporates a chlorine atom into a substituted allylic group, allows for diverse synthesis routes and functionalization possibilities.
  • Potential Use in Synthesis: This compound can serve as a building block in organic synthesis, particularly in the formation of more complex molecules. Its reactivity can be exploited in the production of other fine chemicals and pharmaceuticals.
  • Reactivity and Chemistry: The presence of the double bond in the butenyl group allows for electrophilic addition reactions. Additionally, the chlorine atom may participate in nucleophilic substitutions, making it useful in the synthesis of chlorinated products.
  • Biological Relevance: Compounds similar to 3-chlorobut-2-enylbenzene have shown biological activity in some studies, and could thus be examined for potential therapeutic applications or as agrochemicals.
  • Environmental Impact: The stability of chlorinated organic compounds raises important questions about environmental persistence. Understanding how 3-chlorobut-2-enylbenzene degrades in various conditions is crucial for assessing its ecological footprint.

In summary, while 3-chlorobut-2-enylbenzene may not be among the most widely discussed compounds, its unique structure and chemical properties provide a wealth of opportunities for investigation and practical application. As with many chemicals, further studies could reveal surprising potential!

Synonyms
(3-Chloro-2-buten-1-yl)benzene
15854-63-4
SCHEMBL23406425
SCHEMBL25228665
DTXSID301306187