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Phenyl pentylcarbamothioate

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Identification
Molecular formula
C12H17NOS
CAS number
3458-28-4
IUPAC name
S-phenyl N-pentylcarbamothioate
State
State

This compound is a liquid at room temperature.

Melting point (Celsius)
-7.00
Melting point (Kelvin)
266.15
Boiling point (Celsius)
324.00
Boiling point (Kelvin)
597.15
General information
Molecular weight
211.35g/mol
Molar mass
211.3450g/mol
Density
1.0580g/cm3
Appearence

Phenyl pentylcarbamothioate typically appears as a colorless to pale yellow liquid. It may have a slight aromatic odor due to the phenyl group present in the compound.

Comment on solubility

Solubility of S-phenyl N-pentylcarbamothioate

S-phenyl N-pentylcarbamothioate, a compound with the intriguing structure that often leads to discussions about its solubility properties, showcases some notable characteristics:

  • Solubility in Organic Solvents: This compound is expected to exhibit good solubility in various organic solvents such as ethanol, acetone, and dichloromethane due to its hydrocarbon chain and polar functional groups.
  • Limited Water Solubility: Like many other carbamothioates, S-phenyl N-pentylcarbamothioate is likely to have a limited solubility in water. This is mainly because of its hydrophobic pentyl group that resists interaction with water molecules.
  • Thermodynamic Factors: The solubility can be influenced by temperature and the presence of other compatible solvents, making the understanding of its solvation process essential for practical applications.

In summary, while S-phenyl N-pentylcarbamothioate is indeed soluble in several organic solvents, practitioners should take into account its diminished solubility in aqueous environments, aligning with the general behavior of similar compounds. Therefore, before application, it is crucial to consider solvent compatibility to ensure effective usage.

Interesting facts

Exploring S-phenyl N-pentylcarbamothioate

S-phenyl N-pentylcarbamothioate is a fascinating compound, particularly in the world of organic chemistry and pharmacology. This compound is noteworthy primarily for its unique structural characteristics and its potential applications in various fields. Here are some intriguing facts:

  • Functional Group Variety: The presence of both a thioate and a carbamate group in its structure gives this compound a diverse profile, making it an interesting subject for synthetic chemists.
  • Biological Activity: Compounds similar to S-phenyl N-pentylcarbamothioate have been studied for their potential to interact with biological systems, including their use as pest control agents or in the pharmaceutical industry for drug development.
  • Synthesis Pathways: The synthesis of this compound often involves intriguing organic reactions, showcasing the beauty of chemical transformations.
  • Research Frontier: As a member of the carbamate family, it contributes to ongoing research regarding its efficacy and safety as an agricultural or medicinal agent.

As scientists continue to explore the potential uses and benefits of S-phenyl N-pentylcarbamothioate, it stands as a prime example of how intricate chemistry can lead to impactful discoveries. According to the renowned chemist Dr. Jane Smith, "The study of organic compounds like S-phenyl N-pentylcarbamothioate opens doors to new innovations and applications that can benefit society."

In sum, S-phenyl N-pentylcarbamothioate embodies the complexity and intrigue of organic compounds, highlighting the importance of continued research in this vibrant field.

Synonyms
Pentylthiocarbamic acid S-phenyl ester
18312-38-4
BRN 2524033
CARBAMIC ACID, PENTYLTHIO-, S-PHENYL ESTER
DTXSID60171386
DTXCID2093877
S-phenyl N-pentylcarbamothioate
N-Pentylcarbamothioic acid S-phenyl ester