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S-(p-tolyl) 4-nitrobenzenecarbothioate

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Identification
Molecular formula
C14H11NO3S
CAS number
1887-51-4
IUPAC name
S-(p-tolyl) 4-nitrobenzenecarbothioate
State
State

At room temperature, S-(p-tolyl) 4-nitrobenzenecarbothioate is in a solid state. It is typically stable under normal conditions of temperature and pressure.

Melting point (Celsius)
90.00
Melting point (Kelvin)
363.00
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.00
General information
Molecular weight
275.33g/mol
Molar mass
275.3340g/mol
Density
1.3000g/cm3
Appearence

S-(p-tolyl) 4-nitrobenzenecarbothioate appears as a yellow crystalline solid. It is typically presented in powder form and may exhibit a glossy or matte surface depending on the purity and crystallinity of the sample.

Comment on solubility

Solubility of S-(p-tolyl) 4-nitrobenzenecarbothioate

S-(p-tolyl) 4-nitrobenzenecarbothioate is a compound with intriguing solubility characteristics. Understanding its solubility is essential for applications across various fields.

Key Aspects of Solubility:

  • Polar vs. Nonpolar Solvents: This compound is expected to exhibit limited solubility in polar solvents such as water due to its nonpolar hydrocarbon structure and aromatic character. However, it shows better solubility in nonpolar organic solvents.
  • Influence of Functional Groups: The presence of the nitro group adds some polarity, potentially enhancing solubility in certain organic solvents compared to purely nonpolar compounds.
  • Temperature Dependence: Typically, solubility can increase with temperature; therefore, heating the solvent may improve the dissolution process.
  • Concentration Factors: At higher concentrations, interactions between molecules may affect solubility, leading to precipitation or crystallization.

In summary, S-(p-tolyl) 4-nitrobenzenecarbothioate demonstrates a nuanced relationship with solubility, largely influenced by solvent choice and environmental conditions. As a rule of thumb, when experimenting with such compounds, aim to use appropriate solvents to achieve desired concentrations and solubility behavior!

Interesting facts

Interesting Facts about S-(p-tolyl) 4-nitrobenzenecarbothioate

S-(p-tolyl) 4-nitrobenzenecarbothioate is a fascinating compound that has garnered interest for its unique properties and potential applications in various fields. Here are some intriguing aspects of this compound:

  • Thioester Linkage: This compound contains a thioester functional group, which is known for its role in biological processes, particularly in the metabolism of fatty acids. It can be a source of carboxylic acids upon hydrolysis, making it relevant in biological reactions.
  • Diverse Applications: Due to its structure, S-(p-tolyl) 4-nitrobenzenecarbothioate may find utility in fields such as medicinal chemistry and material science. Its derivatives can serve as intermediates in the synthesis of pharmaceuticals and agricultural chemicals.
  • Structural Features: The presence of a nitro group introduces significant electronic effects into the molecule, altering its reactivity and making it an interesting subject for studies on electrophilic substitution reactions.
  • Potential for Green Chemistry: With increasing emphasis on sustainable practices, there is potential for compounds like this to be involved in green chemistry initiatives. Their synthesis and application might lead to more environmentally friendly processes in organic synthesis.
  • Research Opportunities: As a compound that hasn't been extensively studied, S-(p-tolyl) 4-nitrobenzenecarbothioate presents ample opportunities for exploration and discovery in both academic and industrial research.

Quote to remember: "The beauty of chemistry lies in its complexity, where even the simplest structures can lead to profound discovery."

Overall, S-(p-tolyl) 4-nitrobenzenecarbothioate serves as a reminder of the intricacies of chemical compounds and their potential impacts on science and industry.

Synonyms
S-(p-Tolyl) p-nitrothiobenzoate
28122-84-1
BRN 2507646
BENZOIC ACID, p-NITROTHIO-, S-(p-TOLYL) ESTER
DTXSID50182401
S-(p-Tolyl) 4-nitrothiolbenzoate
4-09-00-01399 (Beilstein Handbook Reference)
RefChem:566153
DTXCID20104892
653-086-2
S-(4-Methylphenyl) 4-nitrobenzenecarbothioate
Benzoic acid, p-nitrothio-, S-p-tolyl ester
SCHEMBL31054333
LMFTVBRXQOQHQC-UHFFFAOYSA-N
Benzenecarbothioic acid, 4-nitro-, S-(4-methylphenyl) ester
AKOS024333282
p-Nitrothiobenzoic acid S-p-tolyl ester
4-Nitro-thiobenzoic acid S-p-tolyl ester
s-(4-Methylphenyl)4-nitrobenzenecarbothioate
S-(4-Methylphenyl) 4-nitrobenzenecarbothioate #