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Benzarone

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Identification
Molecular formula
C13H11ClOS2
CAS number
16111-59-6
IUPAC name
1-(4-chlorophenyl)-3-(decylamino)propane-1,1-dithiol
State
State

Benzarone is typically a solid at room temperature.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
365.70
Boiling point (Kelvin)
638.85
General information
Molecular weight
233.50g/mol
Molar mass
233.5000g/mol
Density
1.1100g/cm3
Appearence

Benzarone appears as a crystalline solid. It is generally white or off-white in color.

Comment on solubility

Solubility of 1-(4-chlorophenyl)-3-(decylamino)propane-1,1-dithiol

The solubility of 1-(4-chlorophenyl)-3-(decylamino)propane-1,1-dithiol can be quite interesting due to its complex structure and functional groups.

Here are some key points regarding its solubility:

  • Polar vs. Non-polar: The presence of the decylamino group suggests that this compound possesses significant non-polar characteristics, which may render it poorly soluble in polar solvents like water.
  • Solvent Compatibility: Instead, one would expect better solubility in non-polar solvents such as hexane or chloroform, given the long hydrocarbon chain.
  • Functional Group Influence: The chlorophenyl substituent may also create specific solvation interactions that can further influence its solubility profile.
  • Hydrophobic Interactions: The substantial hydrocarbon chain creates a hydrophobic character that may limit solubility in hydrophilic environments.

In conclusion, while 1(4-chlorophenyl)-3-(decylamino)propane-1,1-dithiol may demonstrate limited solubility in polar solvents, it is likely to dissolve well in non-polar solvents due to its overall non-polar characteristics and hydrophobicity. Therefore, understanding its solubility is essential for applications in various chemical contexts.

Interesting facts

Interesting Facts About 1-(4-Chlorophenyl)-3-(decylamino)propane-1,1-dithiol

This intriguing compound, 1-(4-chlorophenyl)-3-(decylamino)propane-1,1-dithiol, offers a fascinating glimpse into the world of organic chemistry, particularly in the realm of **thiol compounds**. Here are some noteworthy aspects:

  • Thiol Significance: The presence of thiol (-SH) groups in this compound contributes to its potential reactivity, exhibiting properties essential for various chemical reactions, such as nucleophilic substitution and redox chemistry.
  • Biological Relevance: Compounds containing thiol groups are known to play critical roles in biological systems, participating in protein folding and enzyme activity, indicating the potential biological activities of this compound.
  • Structural Diversity: The unique structure, which includes a decyl chain, suggests applications in **drug design** and **materials science**. The hydrophobic decyl group can influence the compound's interaction with biological membranes, potentially affecting its bioavailability.
  • Chlorophenyl Influence: The 4-chlorophenyl moiety may provide interesting electronic properties, which could enhance the compound's ability to interact with receptors or other biological targets. As quoted by researchers, “The introduction of electron-withdrawing groups can significantly alter the biological activity of compounds.”

As a **chemical scientist** or chemistry student, one might explore further on:

  1. Potential antiviral or antibacterial properties that such compounds may exhibit.
  2. A possible method for synthesizing similar thiol-containing compounds using a **green chemistry** approach, minimizing environmental impact.
  3. The mechanism of action of this compound's functional groups in biological contexts.

In summary, 1-(4-chlorophenyl)-3-(decylamino)propane-1,1-dithiol serves as a fascinating compound that straddles the line between theory and practicality, invoking curiosity in medicinal and environmental chemistry alike.