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Thiocarbanilide

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Identification
Molecular formula
C8H9NS
CAS number
102-08-9
IUPAC name
S-methyl N-phenylcarbamothioate
State
State

At room temperature, thiocarbanilide is typically in a solid state. It can be found as crystalline particles that are usually stable if kept under normal conditions.

Melting point (Celsius)
154.00
Melting point (Kelvin)
427.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
183.29g/mol
Molar mass
214.3290g/mol
Density
1.2130g/cm3
Appearence

Thiocarbanilide appears as a white to pale yellow crystalline solid. It is typically odorless and can be noted for its fine and granular texture. The compound is stable under normal temperatures and pressures.

Comment on solubility

Solubility of S-methyl N-phenylcarbamothioate

S-methyl N-phenylcarbamothioate, with its unique chemical structure, demonstrates varying solubility characteristics that are worth noting. Here are some insights into its solubility:

  • Solvent Dependency: The solubility of this compound is highly dependent on the solvent used. It tends to dissolve better in organic solvents like ethanol and acetone, rather than in polar solvents such as water.
  • Temperature Effects: Like many organic compounds, its solubility can increase with temperature, making it more soluble in warmer conditions.
  • Chemical Interactions: The presence of polar functional groups may enhance its interaction with polar solvents, but the overall characteristics will still lean towards lower solubility in water.
  • Practical Applications: Understanding the solubility profile of S-methyl N-phenylcarbamothioate is crucial for its applications in fields such as agriculture and pharmaceuticals, where optimal solubility can affect efficacy.

In summary, while S-methyl N-phenylcarbamothioate exhibits limited solubility in water, its solubility in organic solvents highlights its versatility for various applications. As such, exploring its solubility behavior is essential for optimizing its use in different fields.

Interesting facts

Interesting Facts About S-methyl N-phenylcarbamothioate

S-methyl N-phenylcarbamothioate is a fascinating compound known for its versatility in various applications, particularly in the field of agrochemicals. Here are some noteworthy facts:

  • Chemical Classification: This compound is classified as a thioester, which means it contains a sulfur atom bonded to a carbonyl group. Thioesters are important intermediates in organic synthesis.
  • Biological Activity: S-methyl N-phenylcarbamothioate exhibits insecticidal properties, making it a valuable compound in the development of pesticides aimed at protecting crops from pests.
  • Mechanism of Action: The mode of action involves inhibiting key biochemical pathways in target organisms, which disrupts their normal functioning and ultimately leads to their demise.
  • Research Significance: Scientists are increasingly exploring the potential of carbamate derivatives like S-methyl N-phenylcarbamothioate in medicinal chemistry, particularly for their antifungal and antibacterial properties.
  • Synthesis: The synthesis of this compound typically involves the reaction of phenyl isocyanate with methyl thiol, followed by specific purification processes to obtain the final product.

Overall, S-methyl N-phenylcarbamothioate serves as an intriguing example of how chemical compounds can have significant impacts in both agriculture and medicine, underscoring the importance of ongoing research in this field. As the quote goes, "Research is creating new knowledge." This compound indeed exemplifies the innovative spirit of chemical science!

Synonyms
S-Methyl thiocarbanilate
S-methyl N-phenylcarbamothioate
13509-38-1
Carbamothioic acid, phenyl-, S-methyl ester
CARBANILIC ACID, THIO-, S-METHYL ESTER
Phenylthiocarbamic acid S-methyl ester
S-Methyl phenylcarbamothioate
S-Methyl phenylthiocarbamate
BRN 2803059
AI3-33177
Carbamothioic acid, phenyl-, S-methyl ester (9CI)
S-methyl anilinomethanethioate
0-12-00-00386 (Beilstein Handbook Reference)
S-Methyl phenylthiocarbamate #
SCHEMBL7258589
SCHEMBL10964505
DTXSID40159248
PUIULWGWXRSXTC-UHFFFAOYSA-N