2-Ethylpyridine-4-carboximidothioic acid

Identification

Molecular formula

C₈H₁₀N₂S

CAS number

2288-01-9

IUPAC name

2-ethylpyridine-4-carboximidothioic acid

State

At room temperature, 2-ethylpyridine-4-carboximidothioic acid is in a solid state. Its crystalline form is stable under normal conditions but may react when exposed to specific environmental factors such as humidity and light.

Melting point (Celsius)

81.20

Melting point (Kelvin)

354.35

Boiling point (Celsius)

190.30

Boiling point (Kelvin)

463.45

General information

Molecular weight

182.18g/mol

Molar mass

182.1840g/mol

Density

1.0927g/cm³

Appearence

2-Ethylpyridine-4-carboximidothioic acid usually appears as a crystalline solid. Its appearance can vary from slightly off-white to a pale yellow color. It is sensitive to air and moisture, which may lead to a change in its appearance upon exposure.

Comment on solubility

Solubility of 2-ethylpyridine-4-carboximidothioic acid

2-ethylpyridine-4-carboximidothioic acid (C₈H₁₀N₂S) is a compound with interesting solubility characteristics. The solubility of this compound can be influenced by various factors, including:

Polarity: The presence of both the carboximidothioic and pyridine functional groups contributes to its polarity, which can enhance its solubility in polar solvents such as water and alcohols.
Functional Groups: Functional groups like thiol or amine groups generally increase solubility in aqueous environments due to their ability to form hydrogen bonds.
Temperature: As with many organic compounds, solubility tends to increase with temperature, making hot solvents a useful method to facilitate dissolution.

Despite these influencing factors, it is important to note that 2-ethylpyridine-4-carboximidothioic acid may exhibit limited solubility in non-polar solvents, which results from its more polar structure. Generally, the solubility of compounds is also dependent on the presence of impurities or the ionic strength of the solvent. As with many organic compounds, understanding the solubility characteristics is crucial for applications, including synthesis and formulation processes.

Interesting facts

Interesting Facts about 2-Ethylpyridine-4-carboximidothioic Acid

2-Ethylpyridine-4-carboximidothioic acid is a fascinating compound with several noteworthy characteristics that make it an interesting subject of study in the field of chemistry.

Biological Significance

This compound has potential applications in medicinal chemistry, particularly in the synthesis of novel therapeutic agents.
Its structure suggests a possible interaction with biological systems, making it a candidate for research into anti-inflammatory or anti-cancer properties.

Synthetic Applications

2-Ethylpyridine-4-carboximidothioic acid can serve as a versatile precursor in organic synthesis, allowing for the creation of more complex molecules.
The presence of both thiol and imido functional groups in its structure makes it an important building block for heterocyclic compounds.

Unique Features

The compound contains a pyridine ring, which is known for its ability to participate in various chemical reactions due to its electron-withdrawing nitrogen atom.
It combines *both* carboxylic acid and imine functionalities, granting it unique reactivity that can be exploited in chemical reactions.

Fun Fact: The reaction pathways that 2-ethylpyridine-4-carboximidothioic acid can undergo are of great interest, particularly due to its potential role as a ligand in coordination chemistry.

Overall, 2-ethylpyridine-4-carboximidothioic acid showcases the intricate and diverse chemistry that can stem from relatively simple compounds, underscoring the value of studying them in various applications.