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3-allylsulfinylprop-1-ene-1-thiol

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Identification
Molecular formula
C6H10OS2
CAS number
7500-06-5
IUPAC name
3-allylsulfinylprop-1-ene-1-thiol
State
State

This compound is generally found in the liquid state at room temperature. It is easily handled in typical laboratory conditions.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
145.00
Boiling point (Kelvin)
418.15
General information
Molecular weight
146.23g/mol
Molar mass
146.2320g/mol
Density
1.0120g/cm3
Appearence

3-allylsulfinylprop-1-ene-1-thiol is a liquid compound with a pale yellow to colorless appearance. It may possess a distinct, often pungent, garlic or onion-like odor, typical of sulfur-containing organic compounds.

Comment on solubility

Solubility of 3-allylsulfinylprop-1-ene-1-thiol (C6H10OS2)

The solubility of 3-allylsulfinylprop-1-ene-1-thiol is an intriguing topic due to the presence of multiple functional groups that can influence its interaction with solvents. This compound contains both thiol and sulfinyl functional groups, which are known to exhibit distinct solubility behaviors. Here’s a breakdown of the factors affecting its solubility:

  • Polarity: The thiol group (-SH) generally enhances solubility in polar solvents due to its ability to form hydrogen bonds.
  • Hydrophobic Character: The allyl group contributes to a certain degree of hydrophobicity, which can limit solubility in highly polar environments.
  • Solvent Interactions: The compound may exhibit better solubility in moderate polar solvents, such as alcohols or some ethers, where both polar and non-polar interactions can occur.

In practice, 3-allylsulfinylprop-1-ene-1-thiol is likely to be soluble in:

  1. Polar aprotic solvents (e.g., acetone, DMSO)
  2. Alcohols (to varying extents, depending on the specific alcohol used)
  3. Some organic solvents that can stabilize the thiol and sulfinyl moieties.

However, it may show limited solubility in non-polar solvents such as hydrocarbons, reflecting the balance between its polar and non-polar characteristics.
In conclusion, understanding the solubility profile of 3-allylsulfinylprop-1-ene-1-thiol is essential for its applications in various chemical and pharmaceutical domains.

Interesting facts

Discovering 3-Allylsulfinylprop-1-ene-1-thiol

3-Allylsulfinylprop-1-ene-1-thiol, often referred to in the context of organosulfur chemistry, presents a fascinating combination of functional groups that make it a remarkable compound for study. Here are some intriguing aspects of this compound:

  • Unique Structure: The presence of both allyl and sulfinyl groups within its structure contributes to its reactivity and potential applications in organic synthesis.
  • Natural Occurrence: This compound belongs to a larger class of thials and sulfoxides, which can occur naturally in certain plants, suggesting a role in plant biochemistry.
  • Chemical Reactivity: The nucleophilic thiol group (–SH) makes it an excellent candidate for reactions such as thiol-ene chemistry, which is significant in developing new materials.
  • Biological Significance: Compounds containing sulfur, like 3-allylsulfinylprop-1-ene-1-thiol, are often studied for their antimicrobial properties and potential health benefits.

As a student or researcher, one might say, “The chemistry of sulfur compounds opens new avenues for innovation in both pharmaceuticals and materials science.” This compound serves as a prime example of how organosulfur compounds can bridge multiple disciplines, including medicinal chemistry, organic synthesis, and even agricultural chemistry.

In essence, studying 3-allylsulfinylprop-1-ene-1-thiol not only enhances our understanding of chemical reactions involving sulfur but may also unveil novel applications across various scientific fields.

Synonyms
SCHEMBL4329032
3-(allylsulfinyl)prop-1-ene-1-thiol
PD042194