2-Ethylpyridine-4-carboximidothioic acid

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Identification

Molecular formula
C8H10N2S
CAS Number
2288-01-9
IUPAC Name
2-ethylpyridine-4-carboximidothioic acid
Molecular Weight
182.18g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0927g/cm3
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.
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.

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