Skip to main content

2-Isopropyl-1,3-dithiolane

ADVERTISEMENT
Identification
Molecular formula
C6H12S2
CAS number
35230-64-1
IUPAC name
2-isopropyl-1,3-dithiolane
State
State

In its pure form, 2-isopropyl-1,3-dithiolane exists as a liquid at room temperature. It remains stable in its liquid form under normal atmospheric conditions.

Melting point (Celsius)
-68.00
Melting point (Kelvin)
205.15
Boiling point (Celsius)
193.50
Boiling point (Kelvin)
466.60
General information
Molecular weight
148.28g/mol
Molar mass
148.2830g/mol
Density
1.0245g/cm3
Appearence

2-Isopropyl-1,3-dithiolane is typically a colorless liquid under standard conditions. Its appearance can be described as clear and free from impurities when relatively pure.

Comment on solubility

Solubility of 2-isopropyl-1,3-dithiolane

2-isopropyl-1,3-dithiolane is a unique organic compound featuring intriguing solubility characteristics. Its solubility is influenced by various factors, including:

  • Polarity: The presence of sulfur atoms contributes to the overall polarity of the molecule, allowing it to interact with polar solvents.
  • Hydrophobicity: The isopropyl group introduces a non-polar element, which can limit solubility in very polar solvents.
  • Temperature: As with many organic compounds, solubility can increase with temperature, making it beneficial for dissolving in warmer solutions.

In general, 2-isopropyl-1,3-dithiolane tends to be soluble in organic solvents such as:

  • Alcohols (e.g., ethanol)
  • Aromatic hydrocarbons (e.g., toluene)
  • Chloroform

However, it is less likely to dissolve in water due to its hydrophobic characteristics. Thus, when working with this compound, it is essential to choose the right solvent for optimal solubility. Always remember, "Solubility is not just a measure of how much can dissolve, but also a dance between molecular structures!"

Interesting facts

Interesting Facts about 2-isopropyl-1,3-dithiolane

2-isopropyl-1,3-dithiolane is a fascinating compound that belongs to the class of dithiolanes — a group notable for their unique chemical properties and structural characteristics. Here are some engaging insights into this intriguing compound:

  • Structural Composition: This compound features a five-membered ring containing two sulfur atoms. This unique arrangement gives 2-isopropyl-1,3-dithiolane its distinctive properties that are not found in more common hydrocarbon structures.
  • Versatile Applications: The presence of dithiolane in its structure makes the compound useful in a variety of fields. Its derivatives have found applications in organic synthesis, particularly in the production of other sulfur-containing compounds, which are pivotal in pharmaceuticals and agrochemicals.
  • Odor Characteristics: Compounds in this class are often known for their strong and sometimes pungent odors. This makes them interesting to study in the context of olfactory chemistry, where the sensory qualities of compounds can greatly influence their application.
  • Reactivity: The position of the isopropyl group offers unique reactivity. The steric hindrance of the isopropyl group can influence how the dithiolane participates in chemical reactions, leading to selective reactions that are advantageous in synthetic chemistry.
  • Research Interest: 2-isopropyl-1,3-dithiolane has garnered interest in recent research for its potential in developing new materials and compounds with specific functionalities, such as catalysts or stabilizing agents.

As we delve deeper into the properties and applications of 2-isopropyl-1,3-dithiolane, we uncover not only its significance in synthetic chemistry but also the broader implications for developing innovative compounds in various scientific fields.

Synonyms
2-Isopropyl-1,3-dithiolane
1,3-DITHIOLANE, 2-ISOPROPYL-
26733-24-4
N1LQ3M3CQT
NSC-193356
NSC 193356
BRN 1420961
2-isopropyl-[1,3]dithiolane
NSC193356
UNII-N1LQ3M3CQT
SCHEMBL3091772
SCHEMBL9672763
DTXSID20181244
2-(1-methylethyl)-1,3-dithiolane
1,3-Dithiolane, 2-(1-methylethyl)-