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S-(4-nitrophenyl) ethanethioate

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Identification
Molecular formula
C8H7NO3S
CAS number
26644-53-5
IUPAC name
S-(4-nitrophenyl) ethanethioate
State
State

At room temperature, S-(4-nitrophenyl) ethanethioate is in a solid state. It is stable under normal conditions but should be stored in a cool, dry place away from light to prevent degradation.

Melting point (Celsius)
69.50
Melting point (Kelvin)
342.65
Boiling point (Celsius)
363.30
Boiling point (Kelvin)
636.45
General information
Molecular weight
197.23g/mol
Molar mass
197.2280g/mol
Density
1.3380g/cm3
Appearence

S-(4-nitrophenyl) ethanethioate appears as a pale yellow to yellow crystalline solid. It may sometimes have a faint aroma due to its thiocarbonyl group, typical of thioesters. The compound is sensitive to photodegradation and may darken upon exposure to light.

Comment on solubility

Solubility of S-(4-nitrophenyl) ethanethioate

S-(4-nitrophenyl) ethanethioate, with its intriguing chemical structure, exhibits specific solubility characteristics that are important for various applications. Understanding its solubility can be quite essential in both laboratory settings and industrial processes. Here’s a closer look at its solubility behavior:

  • Solvent Compatibility: This compound is expected to show good solubility in organic solvents such as ethanol, acetone, and chloroform, which is typical for thioesters.
  • Water Solubility: Generally, S-(4-nitrophenyl) ethanethioate is likely to have limited solubility in water due to its hydrophobic nature imparted by the aromatic nitro group and thiol moiety.
  • Temperature Influence: Solubility may vary with temperature; as temperature increases, solubility in organic solvents might increase, allowing for a more effective dissolution process.
  • pH Effects: The solubility might also be affected by pH levels, particularly when in contact with bases or acids, possibly altering its ionic forms.

In summary, the solubility of S-(4-nitrophenyl) ethanethioate is primarily influenced by the choice of solvent, temperature, and environmental conditions. This compound exemplifies the complex interplay between molecular structure and solubility in different media.

Interesting facts

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.

Synonyms
15119-62-7
p-Nitrophenylthiol acetate
4-Nitrophenylthiol acetate
Ethanethioic acid, S-(4-nitrophenyl) ester
DTXSID70164729
DTXCID6087220
S-(4-nitrophenyl) ethanethioate
S-(p-Nitrophenyl) thioacetate
Benzenethiol, p-nitro-, acetate
ACETIC ACID, THIO-, S-(p-NITROPHENYL) ESTER
S-(4-nitrophenyl) thioacetate
S-(4-nitrophenyl)ethanethioate
SCHEMBL27450016
QCGPFSMQZNLBCA-UHFFFAOYSA-N
AKOS006273244
1-[(4-nitrophenyl)sulfanyl]ethan-1-one
Thioacetic acid S-(4-nitro-phenyl) ester