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Phenyl propyl sulfide

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Identification
Molecular formula
C9H12S
CAS number
1126-78-9
IUPAC name
propylsulfanylbenzene
State
State

Phenyl propyl sulfide is in a liquid state at room temperature.

Melting point (Celsius)
-54.00
Melting point (Kelvin)
219.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
152.27g/mol
Molar mass
152.2650g/mol
Density
1.0043g/cm3
Appearence

Phenyl propyl sulfide is a colorless to pale yellow oily liquid.

Comment on solubility

Solubility of Propylsulfanylbenzene

Propylsulfanylbenzene, also known by its systematic name propylthiophenol or 3-propylthiophenol, exhibits notable solubility characteristics in various solvents. Here are some key points to consider:

  • Solvents: Propylsulfanylbenzene is primarily soluble in organic solvents such as ethanol, acetone, and dichloromethane. This is due to its non-polar characteristics and the presence of the aromatic ring.
  • Water: As for its solubility in water, propylsulfanylbenzene demonstrates low solubility. The non-polar properties of the hydrocarbon moiety hinder its dissolution in polar solvents like water.
  • Influence of Temperature: Increasing temperature typically enhances solubility for many organic compounds. Therefore, raising the temperature of the solvent may improve the dissolution of propylsulfanylbenzene.
  • Comparison with Similar Compounds: Its solubility can be compared to other thiophenols, where the presence of alkyl groups often decreases aqueous solubility and increases solubility in organic solvents.

In summary, while propylsulfanylbenzene is not soluble in water, it shows a significant affinity for organic solvents. This solubility behavior is crucial for its applications in chemical synthesis and production processes.

Interesting facts

Exploring Propylsulfanylbenzene

Propylsulfanylbenzene, also known by its IUPAC name propylthiobenzene, is a fascinating compound that belongs to the family of thiophenes. Here are some engaging facts about this intriguing chemical:

  • Structure and Features: The unique structure of propylsulfanylbenzene consists of a propyl group bonded to a sulfur atom, which is in turn attached to a benzene ring. This makes the compound both organic and distinctively aromatic.
  • Reactivity: As a compound featuring sulfur, propylsulfanylbenzene exhibits interesting reactivity profiles. The thiol group can participate in a range of chemical reactions including oxidation and substitution, which are pivotal in synthetic organic chemistry.
  • Applications: This compound is of particular interest in organic synthesis, serving as a precursor for various derivatives. Its similarities with other sulfides make it valuable for the development of pharmaceuticals and agrochemicals.
  • Odor: Like many sulfur-containing compounds, propylsulfanylbenzene has a distinctive smell that can be quite potent. This characteristic can be both advantageous and disadvantageous depending on its application.
  • Biological Relevance: Compounds containing sulfur are often examined for their biological activities. Research into propylsulfanylbenzene may uncover potential applications in medicinal chemistry and pharmacology.

As we continue to explore the vast universe of organic compounds, propylsulfanylbenzene stands out for its unique properties and the potential it holds in various fields of science. From its intriguing structure to its applications, this compound is indeed remarkable!

Synonyms
Benzene, (propylthio)-
Phenyl propyl sulfide
(Propylthio)benzene
BRN 1857536
DTXSID60236328
4-06-00-01470 (Beilstein Handbook Reference)
Benzene, (propylthio)-(9CI)
DTXCID60158819
nwydlobjqijdgh-uhfffaoysa-n
874-79-3
Phenyl N-propyl sulphide
Propyl phenyl sulfide
propylsulfanylbenzene
(1-Thiabutyl)benzene
n-Propyl phenyl sulfide
SULFIDE, PHENYL PROPYL
Fenyl-propylsulfid
(Propylsulfanyl)benzene
NSC 115079
D272CA2KWS
NSC-115079
Fenyl-propylsulfid [Czech]
Benzene, (propylthio)- (9CI)
phenyl(propyl)sulfane
Phenyl n-propyl sulfide
(Propylsulfanyl)benzene #
UNII-D272CA2KWS
SCHEMBL575835
MFCD00039936
NSC115079
AKOS006243392
DB-057004
10.14272/NWYDLOBJQIJDGH-UHFFFAOYSA-N.1
A842235
doi:10.14272/NWYDLOBJQIJDGH-UHFFFAOYSA-N.1