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1-Allylsulfanyl-N-(3,4-dichlorophenyl)methanimidothioic acid

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Identification
Molecular formula
C11H10Cl2NS2
CAS number
Not Available
IUPAC name
1-allylsulfanyl-N-(3,4-dichlorophenyl)methanimidothioic acid
State
State

This compound is expected to be a solid at room temperature, considering its structural characteristics and molar mass. Its precise crystalline form and properties would depend on the specific isomers and preparation method employed.

Melting point (Celsius)
217.00
Melting point (Kelvin)
490.20
Boiling point (Celsius)
403.50
Boiling point (Kelvin)
676.50
General information
Molecular weight
322.24g/mol
Molar mass
322.2000g/mol
Density
1.2800g/cm3
Appearence

This compound does not have a widely known appearance because it might be less commonly discussed or used compared to some established compounds. Typically, thioic acid derivatives like this might appear as light-colored crystals or powders, but specific details would require experimental verification.

Comment on solubility

Solubility of 1-allylsulfanyl-N-(3,4-dichlorophenyl)methanimidothioic acid

The solubility of 1-allylsulfanyl-N-(3,4-dichlorophenyl)methanimidothioic acid can be influenced by several factors including its molecular structure and functional groups. This compound features both aliphatic and aromatic components, which may affect how it interacts with solvents.

When discussing solubility, consider the following key points:

  • Polarity: Compounds with polar functional groups generally exhibit higher solubility in polar solvents such as water, while non-polar compounds tend to dissolve better in non-polar solvents.
  • Hydrogen Bonds: The presence of functional groups capable of hydrogen bonding can enhance the solubility in polar solvents. For instance, if the compound contains sites that can participate in hydrogen bonding, this could lead to increased solubility.
  • Temperature: Solubility can increase with temperature; thus, examining the specific temperature conditions could provide more insight.
  • pH Level: The solubility might also be affected by the pH of the medium, especially if the compound is ionic or can exist in multiple protonation states.

In conclusion, while the exact solubility of 1-allylsulfanyl-N-(3,4-dichlorophenyl)methanimidothioic acid in various solvents is not provided here, one can infer that its solubility profile would largely depend on the interplay of its molecular characteristics and the solvent properties. As noted, the “like dissolves like” rule is a fundamental principle for predicting solubility outcomes.

Interesting facts

Interesting Facts About 1-Allylsulfanyl-N-(3,4-dichlorophenyl)methanimidothioic Acid

1-Allylsulfanyl-N-(3,4-dichlorophenyl)methanimidothioic acid is a compound that showcases the fascinating chemistry of thioamides and their derivatives. Here are a few key points that make this compound noteworthy:

  • Structural Diversity: This compound contains multiple functional groups, including an allyl group, a sulfenic acid derivative, and a dichlorophenyl group. This structural variability opens up possibilities for numerous chemical reactions and applications.

  • Biological Significance: Compounds featuring sulfur are often studied for their potential biological activities. They may exhibit antimicrobial, antiviral, or anticancer properties, making them interesting candidates in medicinal chemistry.

  • Mechanistic Studies: Understanding the reactivity of such a thioic acid can lead to insights into reaction mechanisms involving sulfur and nitrogen. The interactions of the thioamide functionality can serve as a platform for creating new synthetic pathways.

  • Environmental Impact: As we explore compounds like this one, we also consider their environmental chemistry. The stability and bioactivity of sulfur-containing compounds can influence their behavior in ecological systems, leading to both beneficial and adverse effects.

  • Applications in Material Science: This compound could potentially be used in the synthesis of new materials. The unique properties of sulfur compounds are valuable in creating polymers and other materials with specific characteristics.

In summary, 1-allylsulfanyl-N-(3,4-dichlorophenyl)methanimidothioic acid is not just a simple compound; it embodies the complexity and utility of thioamides in organic chemistry. As research continues, its potential applications could lead to breakthroughs in various scientific fields.