Tryptamine thione | Solubility of Things

Identification

Molecular formula

C₁₂H₁₄N₂S

CAS number

1767-38-4

IUPAC name

N-[2-(1H-indol-3-yl)ethyl]ethanimidothioic acid

State

Tryptamine thione is typically in a solid state at room temperature.

Melting point (Celsius)

180.00

Melting point (Kelvin)

453.15

Boiling point (Celsius)

320.00

Boiling point (Kelvin)

593.15

General information

Molecular weight

189.30g/mol

Molar mass

189.2840g/mol

Density

1.2340g/cm³

Appearence

Tryptamine thione typically appears as a white to off-white powder. It is a crystalline material, usually synthesized for research purposes.

Comment on solubility

Solubility of N-[2-(1H-indol-3-yl)ethyl]ethanimidothioic acid

N-[2-(1H-indol-3-yl)ethyl]ethanimidothioic acid, a compound with a complex structure, presents unique solubility characteristics worthy of exploration. Understanding its solubility is crucial for applications in pharmaceutical and chemical research.

Solubility Characteristics

This compound is expected to demonstrate varying solubility in different solvents:

Water: Generally, compounds with an acid functional group may exhibit moderate solubility in water due to their ability to ionize, although the presence of the indole moiety could hinder extensive solvation.
Organic Solvents: Given the hydrophobic nature of the indole ring, solubility in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), or methanol could be more favorable.
pH Dependency: The solubility might also be affected by the pH of the solution, increasing in more alkaline conditions where deprotonation occurs.

In terms of practical application, the solubility of N-[2-(1H-indol-3-yl)ethyl]ethanimidothioic acid can significantly influence its bioavailability and therapeutic efficacy. Therefore, understanding its behavior in various solvents is essential for optimizing its use.

Interesting facts

Interesting Facts About N-[2-(1H-indol-3-yl)ethyl]ethanimidothioic Acid

N-[2-(1H-indol-3-yl)ethyl]ethanimidothioic acid, often abbreviated as a complex compound of significant interest in the field of medicinal chemistry, stands out due to its unique structure and potential applications. Here are some noteworthy points concerning this intriguing compound:

Structural Significance: This compound features an indole ring, which is a common motif in many biologically active molecules and plays a critical role in various biochemical pathways.
Biological Relevance: Indole derivatives are known for their versatility in pharmacology. N-[2-(1H-indol-3-yl)ethyl]ethanimidothioic acid may exhibit promising biological activities, making it a candidate for drug discovery processes.
Potential Therapeutic Applications: Investigations into similar compounds have revealed anti-inflammatory, anti-cancer, and anti-bacterial properties. While specific studies may be limited, the compound's structural characteristics suggest potential as a therapeutic agent.
Mechanism of Action: The thiol group in its structure could lend to its reactivity, possibly influencing enzymatic pathways or serving as a building block for more complex synthesis.

As with many compounds that exhibit biological activity, further research is essential to fully understand the mechanisms by which N-[2-(1H-indol-3-yl)ethyl]ethanimidothioic acid may operate. Continued exploration could unveil its potential as a significant player in the development of new therapeutic strategies.

In the words of famed chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This compound represents just one of the many ideas circulating in the vast world of chemical research that illustrates the remarkable potential hidden within the realm of organic chemistry.