Skip to main content

S-phenyl 4-chlorobenzenecarbothioate

ADVERTISEMENT
Identification
Molecular formula
C13H9ClOS
CAS number
null
IUPAC name
S-phenyl 4-chlorobenzenecarbothioate
State
State
At room temperature, S-phenyl 4-chlorobenzenecarbothioate is a solid.
Melting point (Celsius)
80.00
Melting point (Kelvin)
353.15
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
248.74g/mol
Molar mass
248.7430g/mol
Density
1.3000g/cm3
Appearence

S-phenyl 4-chlorobenzenecarbothioate appears as a crystalline solid. The crystals are typically off-white to light yellow.

Comment on solubility

Solubility of S-phenyl 4-chlorobenzenecarbothioate

S-phenyl 4-chlorobenzenecarbothioate is an intriguing compound when it comes to its solubility characteristics. The solubility of this compound can be influenced by several factors:

  • Polarity: With a non-polar aromatic structure, the compound tends to have limited solubility in polar solvents like water.
  • Solvent Compatibility: However, it demonstrates better solubility in non-polar organic solvents such as:
    • Chloroform
    • Dichloromethane
    • Ethanol
  • Temperature Effects: Increasing temperature can often enhance solubility in organic solvents.

In summary, while S-phenyl 4-chlorobenzenecarbothioate is likely to be poorly soluble in polar environments, it finds a more favorable environment in non-polar organic solvents, making it essential to choose the right solvent for dissolution and reactions. As always, it is beneficial to conduct solubility tests specific to your conditions to gain precise insights on this compound.

Interesting facts

Interesting Facts about S-phenyl 4-chlorobenzenecarbothioate

S-phenyl 4-chlorobenzenecarbothioate, a thioate compound, showcases an intriguing combination of aromatic chemistry and sulfur functionality. This compound has garnered interest in various fields, including organic synthesis and agrochemicals.

Key Characteristics

  • Functional Group Diversity: The presence of both thioate and aromatic components in S-phenyl 4-chlorobenzenecarbothioate allows for unique reactivity profiles, making it a subject of study for synthetic chemists.
  • Pest Control Applications: Compounds like this one are often explored for their potential use in crop protection, serving as a foundation for designing pesticides that can effectively target specific pests while being environmentally friendly.
  • Structure-Activity Relationship (SAR): Its structural characteristics provide insights into how modifications of the phenyl and chlorobenzene groups can influence biological activity, which is a vital consideration in drug design and development.

Chemical Behavior

Thioates such as S-phenyl 4-chlorobenzenecarbothioate often exhibit interesting chemical behaviors:

  • Nucleophilicity: The sulfur atom can act as a nucleophile, participating in a variety of reactions, including substitutions and additions, which can lead to the formation of new compounds with desirable properties.
  • Stability: The compound's stability under various conditions is an important aspect, particularly in understanding its potential applications in real-world scenarios, such as agricultural use.

Research and Development

Ongoing research into S-phenyl 4-chlorobenzenecarbothioate focuses on:

  • Evaluating its efficacy as a bioactive agent.
  • Investigating its environmental impact and degradation pathways.
  • Improving synthesis methods for better yield and purity.

As a compound with multifaceted uses and potential applications, S-phenyl 4-chlorobenzenecarbothioate is an exciting subject in the landscape of chemistry, bridging the gap between fundamental research and practical innovations.

Synonyms
S-Phenyl p-chlorothiobenzoate
28122-82-9
BENZOIC ACID, p-CHLOROTHIO-, S-PHENYL ESTER
S-phenyl 4-chlorobenzenecarbothioate
BRN 2451949
4-09-00-01392 (Beilstein Handbook Reference)
SCHEMBL8400140
DTXSID90182400
4-Chloro-thiobenzoic acid S-phenyl ester