N,N'-diallylethanediimidothioic acid

Identification

Molecular formula

C₈H₁₄N₂S₂

CAS number

1476-23-9

IUPAC name

N,N'-diallylethanediimidothioic acid

State

At room temperature, N,N'-diallylethanediimidothioic acid is typically found in a liquid state. This compound remains stable as a liquid under standard atmospheric conditions.

Melting point (Celsius)

-33.70

Melting point (Kelvin)

239.45

Boiling point (Celsius)

325.40

Boiling point (Kelvin)

598.55

General information

Molecular weight

187.31g/mol

Molar mass

187.3070g/mol

Density

1.1247g/cm³

Appearence

N,N'-diallylethanediimidothioic acid is generally observed as a yellow or pale-yellow liquid. Its consistency is similar to that of typical organic liquids under room temperature, and it is often found to be oily. The color may vary slightly depending on impurities or the method of synthesis, but it predominantly maintains a light to slightly intense yellow hue.

Comment on solubility

Solubility of N,N'-diallylethanediimidothioic acid

N,N'-diallylethanediimidothioic acid is a compound that exhibits unique solubility characteristics. Understanding its solubility is crucial for applications in various fields such as chemistry and materials science. Here are some key points regarding its solubility:

Water Solubility: This compound is generally poorly soluble in water, which is a typical behavior for thioacids.
Organic Solvents: N,N'-diallylethanediimidothioic acid tends to be more soluble in organic solvents such as ethanol, acetone, and dichloromethane.
pH Effects: The solubility may also vary with pH, as the ionization state of the acid can impact its ability to dissolve in aqueous solutions.
Temperature Influence: An increase in temperature can enhance solubility in organic solvents, beneficial for synthetic applications.

In summary, while N,N'-diallylethanediimidothioic acid exhibits limited solubility in water, it shows a greater affinity for organic solvents, making it versatile for different chemical processes. Remember, the environmental conditions such as temperature and pH can significantly influence its solubility, opening up various avenues for exploration in research and application.

Interesting facts

Interesting Facts about N,N'-diallylethanediimidothioic acid

N,N'-diallylethanediimidothioic acid is a fascinating compound primarily known for its unique structural features and diverse applications in chemistry and material science. Here are some engaging insights:

Thioic Nature: This compound contains thioic acid functional groups, which are sulfur-containing acids, adding to its unique chemical reactivity. The thioic nature of the compound allows it to participate in various chemical reactions that are not possible for standard carboxylic acids.
Imidothioic Integration: The imidothioic moiety in this compound enhances its potential for coordination chemistry. It can form complexes with metals, making it a candidate for use in catalysts or as a ligand in metal complexes.
Applications in Organic Synthesis: Due to the presence of allyl groups, this compound can serve as an important building block in organic synthesis, enabling the formation of more complex molecular architectures through various coupling and cyclization reactions.
Research Interest: Its intriguing structure has garnered attention in research, particularly regarding its biological activity. Compounds with similar structures have been reported to exhibit antimicrobial and anticancer properties.
Versatile Reactivity: N,N'-diallylethanediimidothioic acid can act as a multifunctional agent, allowing for various chemical modifications, thereby increasing its versatility in synthetic chemistry.

In summary, N,N'-diallylethanediimidothioic acid is more than just a compound; it represents a bridge connecting fundamental chemistry to practical applications. Its unique properties not only inspire ongoing research but also demonstrate the profound impact of chemical innovation on various fields.