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Ethyl phenylcarbamodithioate

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Identification
Molecular formula
C9H11NS2
CAS number
10341-31-2
IUPAC name
ethyl(phenyl)carbamodithioic acid
State
State

Liquid at room temperature.

Melting point (Celsius)
16.00
Melting point (Kelvin)
289.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
199.31g/mol
Molar mass
199.3140g/mol
Density
1.1590g/cm3
Appearence

Ethyl phenylcarbamodithioate is generally a pale yellow liquid with a slight aromatic odor.

Comment on solubility

Solubility of Ethyl(phenyl)carbamodithioic Acid

Ethyl(phenyl)carbamodithioic acid, with the chemical formula C9H11NS2, exhibits unique solubility characteristics that are influenced by its structural components. While its solubility can vary widely depending on the solvent, some general observations can be made:

  • Polarity: The presence of the carbamodithioic acid functional group contributes to its polarity, which can enhance its solubility in polar solvents.
  • Solvent Compatibility: It tends to be more soluble in organic solvents such as methanol and ethanol compared to water, primarily due to its hydrophobic ethyl and phenyl groups.
  • Temperature Dependency: As with many organic compounds, an increase in temperature may lead to increased solubility, allowing for better dissolution in non-polar solvents.

In summary, while ethyl(phenyl)carbamodithioic acid shows moderate to good solubility in a variety of organic solvents, it is often less soluble in water. This property can significantly affect its applications and behavior in different chemical environments.

Interesting facts

Interesting Facts About Ethyl(phenyl)carbamodithioic Acid

Ethyl(phenyl)carbamodithioic acid is a fascinating compound that falls within the category of thiourea derivatives. This molecule is characterized by several intriguing properties and applications that highlight its significance in both academic and industrial settings.

Key Properties and Applications

  • Versatile Reactivity: The thiol and amine groups present in ethyl(phenyl)carbamodithioic acid allow for a wide range of chemical reactions, making it an important intermediate in organic synthesis.
  • Pest Control: Research has shown that compounds like this one can exhibit potential as agrochemicals, contributing to effective pest management strategies.
  • Novel Pharmacological Activities: Studies have suggested that derivatives of this compound possess various biological activities, including antimicrobial and anticancer properties.

Chemical Structure Insights

The structural features of ethyl(phenyl)carbamodithioic acid are worth examining:

  • The presence of a carbamodithioic acid group, which contributes to its reactivity.
  • A phenyl group that enhances its ability to interact with biological systems.
  • An ethyl group that influences the solubility and physical properties of the molecule.

The Future of Research

As a compound with promising applications in multiple fields, ongoing research into ethyl(phenyl)carbamodithioic acid could lead to:

  • Newly developed pharmaceutical formulations that leverage its unique properties.
  • Innovative agricultural solutions that are more environmentally friendly.
  • Insights into its mechanism of action, paving the way for the design of targeted drugs.

In summary, ethyl(phenyl)carbamodithioic acid stands out not just as a chemical entity, but as a subject of great interest that bridges the gap between chemistry and practical applications in medicine and agriculture. Its *unique structure* and *reactivity* continue to inspire investigations that may yield exciting discoveries in the near future.

Synonyms
Lead(2+) ethylphenyldithiocarbamate
299-550-4
ethyl(phenyl)carbamodithioic acid
13074-40-3
SCHEMBL1285989
DTXSID10864519
n-ethyl-n-phenyldithiocarbamic acid