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S-(p-tolyl) benzenecarbothioate

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Identification
Molecular formula
C14H12OS
CAS number
18654-81-4
IUPAC name
S-(p-tolyl) benzenecarbothioate
State
State

At room temperature, S-(p-tolyl) benzenecarbothioate is in a solid state, typically appearing as a dry crystalline powder.

Melting point (Celsius)
52.00
Melting point (Kelvin)
325.15
Boiling point (Celsius)
399.00
Boiling point (Kelvin)
672.15
General information
Molecular weight
228.33g/mol
Molar mass
228.3310g/mol
Density
1.1587g/cm3
Appearence

S-(p-tolyl) benzenecarbothioate is a crystalline solid compound. It appears as a white or slightly off-white powder, which can be quite fine in texture. The compound possesses a distinct chemical odor that is characteristic of thioesters.

Comment on solubility

Solubility of S-(p-tolyl) benzenecarbothioate

S-(p-tolyl) benzenecarbothioate, with its unique structure, exhibits interesting solubility characteristics:

  • Solvent Interaction: This compound is likely to show moderate solubility in organic solvents such as ethanol, acetone, and dichloromethane owing to its aromatic components and sulfur atom.
  • Water Solubility: Due to its hydrophobic nature and the presence of bulky groups, S-(p-tolyl) benzenecarbothioate is expected to have limited solubility in water.
  • Temperature Effects: Generally, solubility can increase with temperature, meaning that heating may enhance the dissolution of this compound in suitable organic solvents.
  • pH Dependence: The solubility may also be influenced by the pH of the solution, as changes in ionization state could affect its interactions with solvents.

In summary, while S-(p-tolyl) benzenecarbothioate is not readily soluble in water, its solubility in organic solvents makes it a useful compound in various applications. Experimentation with different solvents is recommended to fully understand its solubility profile.

Interesting facts

Interesting Facts About S-(p-tolyl) Benzenecarbothioate

S-(p-tolyl) benzenecarbothioate is a fascinating compound that belongs to the class of thioesters. This compound is notable for its unique structural features and its applications in various fields. Here are some intriguing details about this chemical:

  • Structural Attributes: S-(p-tolyl) benzenecarbothioate contains a thiol ester functional group, which is known for its reactivity and can participate in numerous chemical reactions, such as nucleophilic substitutions and esterifications.
  • Application in Synthesis: This compound can serve as a pivotal intermediate in organic synthesis, particularly in the creation of more complex molecules. It can be utilized in the synthesis of pharmaceuticals and agrochemicals, expanding its utility in various industries.
  • Biological Significance: Research has shown that thioesters can display interesting biological activities. They may play a role in metabolic processes and are considered for further studies in enzymatic reactions and drug design.
  • Flavor and Fragrance: Thioesters, like S-(p-tolyl) benzenecarbothioate, are often linked to specific flavors and aromas, which could make them valuable in the food and fragrance industries. Their olfactory properties can contribute to the sensory profile of products.

In one study, a researcher noted, “The reactivity of thioesters gives chemists a canvas to explore innovative pathways in synthetic organic chemistry.” This statement highlights the importance of compounds like S-(p-tolyl) benzenecarbothioate in advancing scientific knowledge and applications.

Overall, S-(p-tolyl) benzenecarbothioate exemplifies the remarkable diversity found within chemical compounds and underscores the potential for innovation in both synthetic chemistry and industrial applications.

Synonyms
10371-42-3
S-(4-methylphenyl) benzenecarbothioate
BENZOIC ACID, THIO-, S-(p-TOLYL) ESTER
Thiobenzoic acid S-(4-methylphenyl)
THIOBENZOIC ACID S-P-TOLYL ESTER
S-(p-Tolyl) thiobenzoate
BRN 2049264
s-(4-Methylphenyl)benzenecarbothioate
S-(p-tolyl) benzothioate
SCHEMBL5696801
SCHEMBL9871801
4-methylphenylthio phenyl ketone
DTXSID90146027
thiobenzoic acid S-(p-tolyl) ester
STK701859
AKOS002161601
NCGC00339055-01
ST45188278
AB01330931-02