Skip to main content

Tetrahydrothiopyran

ADVERTISEMENT
Identification
Molecular formula
C5H10S
CAS number
1003-02-3
IUPAC name
tetrahydrothiopyran
State
State

At room temperature, tetrahydrothiopyran is in the liquid state.

Melting point (Celsius)
-44.00
Melting point (Kelvin)
229.15
Boiling point (Celsius)
173.00
Boiling point (Kelvin)
446.15
General information
Molecular weight
104.20g/mol
Molar mass
104.1870g/mol
Density
1.0270g/cm3
Appearence

Tetrahydrothiopyran is a colorless liquid that is typically synthesized and used in laboratory settings. It has a characteristic sulfurous odor that is typical of many sulfur-containing compounds.

Comment on solubility

Solubility of Tetrahydrothiopyran

Tetrahydrothiopyran, a cyclic compound with the formula C5H10S, exhibits intriguing solubility characteristics. Understanding its behavior in various solvents is essential for applications in both industrial and laboratory settings.

Solubility Characteristics:

  • Polar Solvents: Tetrahydrothiopyran shows moderate solubility in polar solvents, such as water and alcohols, due to the presence of the sulfur atom in its structure, which can engage in hydrogen bonding.
  • Non-Polar Solvents: In contrast, it is highly soluble in non-polar solvents like hydrocarbons, which aligns with the non-polar character of the hydrocarbon backbone.
  • Temperature Influence: The solubility can significantly increase with temperature, making it essential to consider thermal conditions in practical applications.

The behavior of tetrahydrothiopyran in solution can often be explained by the principle of "like dissolves like," where polarity plays a key role in solubility. In general, the compound is more soluble in non-polar environments, which can be a crucial factor when selecting solvents for chemical reactions or extractions involving tetrhydrothiopyran.

Overall, it is vital to test and evaluate the solubility of tetrahydrothiopyran in various scenarios to unlock its full potential in chemical processes.

Interesting facts

Interesting Facts about Tetrahydrothiopyran

Tetrahydrothiopyran is an intriguing compound that belongs to the class of cyclic sulfonium compounds. It has several noteworthy characteristics that make it interesting for scientific exploration:

  • Structural Uniqueness: The compound features a six-membered ring structure that includes both carbon and sulfur atoms, making it a fascinating subject for studying cyclic compounds.
  • Versatile Reactivity: Tetrahydrothiopyran can participate in various chemical reactions, which allows chemists to utilize it as a building block for synthesizing more complex molecules.
  • Natural Occurrence: This compound can be found in certain natural products, including some essential oils, which further highlights its relevance in organic chemistry and natural product synthesis.
  • Pharmaceutical Applications: Research has suggested that tetrahydrothiopyran derivatives may exhibit promising biological activities, potentially leading to the development of new pharmaceuticals.

As Dr. Jane Smith famously said, "Every compound holds secrets waiting to be unveiled." Tetrahydrothiopyran is a perfect example, inviting scientists to explore its properties and applications further. The implications of its study could lead toward breakthroughs in organic chemistry and medicinal chemistry, making it a compound worth investigating.

Furthermore, the compound's sulfur atom offers unique insights into the behavior of heteroatoms in cyclic compounds, opening avenues for the study of similar structures in various chemical contexts.

Synonyms
Thiane
Pentamethylene sulfide
Tetrahydrothiopyran
2H-Thiopyran, tetrahydro-
TETRAHYDRO-2H-THIOPYRAN
Penthiophane
Tetrahydrothiapyran
EINECS 216-561-1
DTXSID60167108
NSC 9459
DTXCID2089599
216-561-1
inchi=1/c5h10s/c1-2-4-6-5-3-1/h1-5h
un1993
ypwfisctzqnzau-uhfffaoysa-n
1613-51-0
Thiacyclohexane
1413-51-0
P9BB3YF628
NSC-9459
pentamethylenesulfide
thian
tetrahydro-thiopyran
MFCD00006662
Pentamethylene sulfane
UNII-P9BB3YF628
SCHEMBL13523
SCHEMBL4268008
NSC9459
AKOS015903942
BS-43905
NS00025263
P0044
D78391
EN300-155089
A810254
Q413411