Thiosalicylic acid S-(4-nitrophenyl) ester

Identification

Molecular formula

C₈H₆O₃S₂N

CAS number

123456-78-9

IUPAC name

1-methylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid

State

At room temperature, the compound is typically found as a solid. The robust crystalline structure is characteristic of many aromatic and sulfur-containing organic compounds.

Melting point (Celsius)

105.00

Melting point (Kelvin)

378.15

Boiling point (Celsius)

320.50

Boiling point (Kelvin)

593.65

General information

Molecular weight

244.31g/mol

Molar mass

244.3090g/mol

Density

1.3200g/cm³

Appearence

The compound appears as a yellow crystalline solid that is sensitive to light and moisture. Its crystalline nature often results in well-formed structures, enhancing its purity when freshly prepared.

Comment on solubility

Solubility of 1-methylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid

The solubility of 1-methylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid can be influenced by various factors, primarily due to its unique molecular structure. Here are some important points to consider:

Polarity: The presence of both a nitrophenyl group and a thiol functional group contributes to the polarity of the compound, which generally enhances solubility in polar solvents like water.
Hydrogen bonding: The carboxylic acid moiety can participate in hydrogen bonding, potentially increasing solubility in protic solvents.
Solvent considerations: While it may dissolve well in organic solvents such as ethanol or dimethyl sulfoxide (DMSO), its solubility in nonpolar solvents may be quite limited.
pH effect: Its solubility may also vary with changes in pH, as protonation and deprotonation can alter its charge and thus its solubility profile.

In summary, while 1-methylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid is likely to have good solubility in polar solvents due to its functional groups, its overall solubility characteristics can be quite complex. Understanding these factors can help guide practical applications and experiments.

Interesting facts

Exploring 1-Methylsulfanyl-N-(4-nitrophenyl)methanimidothioic Acid

1-Methylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid is a captivating compound that draws attention due to its unique structural features and potential applications in various fields of research. Here are some key points to consider:

Functional Groups: This compound contains both a nitro group and a thiol component, making it an interesting subject for studies on reactivity and bonding. The presence of the ^−NO₂ group is particularly noteworthy, given its role in electron-withdrawing properties which can significantly influence the compound's reactivity.
Biological Significance: Compounds with similar structures are often explored for their biological activities, such as antimicrobial or anti-inflammatory properties. This opens up fascinating avenues for pharmacological research.
Synthesis Potential: The synthesis of this compound may involve various methods, showcasing the versatility of modern synthetic chemistry. Techniques such as nucleophilic substitution or coupling reactions could be utilized effectively here.
Complex Formation: The thiol (-SH) group in the structure can readily participate in the formation of metal complexes, which could lead to applications in catalysis or materials science.
Environmental Applications: The nature of this compound may allow it to be used in biochemical sensors or pollutants detection, giving it potential relevance in environmental chemistry.

In summary, 1-methylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid is not just a chemical formula but a gateway to understanding advanced concepts in organic chemistry, pharmacology, and materials science. As researchers delve further into its properties and potentials, we can expect exciting developments that could pave the way for new innovations!