N-(3,4-dichlorobenzoyl)-1-methoxy-methanimidothioic acid

Identification

Molecular formula

C₉H₈Cl₂NO₂S

CAS number

563-72-4

IUPAC name

N-(3,4-dichlorobenzoyl)-1-methoxy-methanimidothioic acid

State

This compound is typically in a solid state at room temperature. Being a crystalline solid, it will not flow like liquids, nor will it expand to fill containers like gases. Its rigidity is characteristic of solids.

Melting point (Celsius)

112.00

Melting point (Kelvin)

385.15

Boiling point (Celsius)

350.00

Boiling point (Kelvin)

623.15

General information

Molecular weight

280.14g/mol

Molar mass

280.1400g/mol

Density

1.4800g/cm³

Appearence

The compound appears as a crystalline solid with a distinct structure due to its chemical composition. Generally, compounds of this nature may range from white to off-white in color and may exhibit some degree of luster. The crystal structure may also be noted for its precision in research settings.

Comment on solubility

Solubility of N-(3,4-dichlorobenzoyl)-1-methoxy-methanimidothioic acid

N-(3,4-dichlorobenzoyl)-1-methoxy-methanimidothioic acid is a fascinating compound when it comes to solubility. Its solubility can be influenced by several factors, which are important to understand:

Polarity: The presence of both polar and non-polar functional groups can lead to variances in solubility in various solvents.
Hydrogen Bonding: This compound can potentially engage in hydrogen bonding which may enhance its solubility in polar solvents such as water.
Temperature: Solubility often increases with temperature; thus, heating the solvent could improve the dissolution process.
Solvent Type: Non-polar solvents may not dissolve this compound well due to its polar characteristics, thus leading to limited solubility.

In summary, the solubility of N-(3,4-dichlorobenzoyl)-1-methoxy-methanimidothioic acid can be categorized as moderate to low in water, while it may exhibit better solubility in organic solvents. Specific experimental conditions are essential in determining its exact solubility profile.

Interesting facts

Interesting Facts about N-(3,4-Dichlorobenzoyl)-1-methoxy-methanimidothioic acid

N-(3,4-Dichlorobenzoyl)-1-methoxy-methanimidothioic acid is a fascinating compound with a variety of applications and chemical behaviors that make it a subject of interest in the field of chemistry. Here are some noteworthy points about this compound:

Structural Diversity: This compound contains functional groups like thioic acid and methoxy, which contribute to its unique reactivity and interaction with biological systems.
Pharmaceutical Relevance: Compounds similar to N-(3,4-Dichlorobenzoyl)-1-methoxy-methanimidothioic acid have been investigated for their potential use in medicinal chemistry. The presence of the dichlorobenzoyl moiety in the structure can influence biological activity, opening pathways for the development of new therapeutic agents.
Environmental Studies: The incorporation of halogens such as chlorine into organic compounds often results in increased stability and persistence in the environment. Understanding how such compounds break down and interact with other chemicals is crucial for environmental chemists.
Synthesis Challenges: The synthesis of this compound can be quite intricate due to its multi-functional nature. Chemists must carefully consider reaction conditions to ensure the integrity of the sensitive functional groups.
Analytical Techniques: The characterization of N-(3,4-dichlorobenzoyl)-1-methoxy-methanimidothioic acid often requires sophisticated analytical methods such as NMR spectroscopy and mass spectrometry, which reveal important details about its structure and purity.

Overall, N-(3,4-Dichlorobenzoyl)-1-methoxy-methanimidothioic acid serves as a compelling example of how complex organic molecules play a role in diverse scientific fields, from pharmaceuticals to environmental chemistry. As we strive to understand and manipulate such compounds, we uncover not only their potential benefits but also the intricate chemistry that governs their behavior.