S-(4-nitrophenyl) ethanethioate
- Molecular formula
- C8H7NO3S
- CAS Number
- 26644-53-5
- IUPAC Name
- S-(4-nitrophenyl) ethanethioate
- Molecular Weight
- 197.23g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3380g/cm3
- Synonyms
- 15119-62-7
Identification
Interesting Facts about S-(4-nitrophenyl) ethanethioate
S-(4-nitrophenyl) ethanethioate is an intriguing compound that combines elements of organic chemistry and biochemistry. It is part of a larger family of thioester compounds, which play significant roles in various biochemical reactions.
Key Characteristics
- Functional Group: This compound contains a thioester functional group, which is essential in biochemical processes such as fatty acid metabolism.
- Role in Organic Synthesis: S-(4-nitrophenyl) ethanethioate serves as an important intermediate in the synthesis of more complex organic molecules. Its reactivity allows for the introduction of significant functional groups in synthetic routes.
Applications in Research
The unique properties of this compound make it a subject of interest in various research fields:
- Pesticide Development: Compounds with similar structures are often evaluated for their potential as pesticides due to their reactivity towards biological target sites.
- Biochemical Studies: Researchers use S-(4-nitrophenyl) ethanethioate to study enzyme mechanisms, specifically those involving thioester bonds.
Safety and Handling
As with many organic compounds, it is crucial to handle S-(4-nitrophenyl) ethanethioate with care:
- Proper Personal Protective Equipment (PPE): Always wear gloves and goggles when handling to avoid skin and eye irritation.
- Well-Ventilated Area: Conduct experiments in a fume hood to minimize inhalation risks.
In summary, S-(4-nitrophenyl) ethanethioate is more than just a chemical compound; it connects various fields of chemistry and biology. Its applications in organic synthesis and research show the importance of thioesters in scientific advancements.