Methiothepin | Solubility of Things

Identification

Molecular formula

C₁₉H₂₃N₁O₁S₂

CAS number

18699-02-0

IUPAC name

N-[2,6-bis(methylsulfanyl)phenyl]-2-(diethylamino)acetamide

State

At room temperature, Methiothepin is typically in a solid state.

Melting point (Celsius)

128.00

Melting point (Kelvin)

401.15

Boiling point (Celsius)

315.00

Boiling point (Kelvin)

588.15

General information

Molecular weight

385.56g/mol

Molar mass

385.5630g/mol

Density

1.2503g/cm³

Appearence

Methiothepin typically appears as a crystalline solid with a pale yellow to off-white color.

Comment on solubility

Solubility of N-[2,6-bis(methylsulfanyl)phenyl]-2-(diethylamino)acetamide

N-[2,6-bis(methylsulfanyl)phenyl]-2-(diethylamino)acetamide, with the chemical formula C₁₉H₂₃N₁O₁S₂, presents some intriguing characteristics regarding its solubility.

This compound is typically regarded as having moderate solubility in organic solvents due to the presence of both polar and non-polar functional groups. The key factors influencing its solubility include:

Polar Amino Group: The diethylamino group contributes to the compound's ability to dissolve in polar solvents, such as water, to a certain extent.
Non-Polar Hydrocarbon Regions: The presence of alkyl chains and the phenyl ring provides hydrophobic character, which can enhance solubility in non-polar solvents.
Sulfanyl Substituents: The methylsulfanyl groups may also interact with solvent molecules, affecting solubility in different media.

As a general rule, compounds with more polar functional groups tend to have better solubility in water, while those dominated by hydrocarbon structures favor organic solvents like ethanol or chloroform.

In summary, the solubility of N-[2,6-bis(methylsulfanyl)phenyl]-2-(diethylamino)acetamide can be described as a delicate balance between its polar and non-polar regions. When using this compound in practical applications, it is essential to consider the solvent type to achieve optimal dissolution:

Water: Limited solubility
Ethanol: Moderate solubility expected
Chloroform: Likely higher solubility

Understanding the solubility profile of this compound can greatly enhance its utility in various chemical applications.

Interesting facts

Interesting Facts about N-[2,6-bis(methylsulfanyl)phenyl]-2-(diethylamino)acetamide

N-[2,6-bis(methylsulfanyl)phenyl]-2-(diethylamino)acetamide is a fascinating compound known for its diverse applications in the field of organic chemistry and medicinal research. Here are some insightful points about this intriguing molecule:

Complex Structure: This compound features a unique arrangement that includes a bis(methylsulfanyl)phenyl group, which adds a significant degree of complexity and potential for reactivity.
Potential Biological Activity: Compounds with similar structures are often investigated for their biological properties, including antitumor and antimicrobial activities. The presence of sulfur atoms in the structure can enhance interactions with biological targets.
Drug Development: The diethylamino acetamide moiety is a common motif in pharmaceuticals. Scientists often explore its effectiveness in the development of new therapeutic agents, especially in the fields of pain management and neurological disorders.
Reactivity: The functional groups present in this compound suggest various possible reactions. Understanding these reactions can lead to the synthesis of novel derivatives that may display enhanced properties.
Analytical Studies: This compound serves as a solid subject for analytical chemistry. Techniques such as NMR spectroscopy and mass spectrometry can be employed to study its structural characteristics and confirm its identity.
Environmental Impact: Emerging research suggests that compounds with sulfur-containing groups may have unique environmental interactions, which could be essential for ecotoxicology studies.

With its rich chemical nature and potential pharmacological applications, N-[2,6-bis(methylsulfanyl)phenyl]-2-(diethylamino)acetamide provides an exciting landscape for future research endeavors.