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1-allylsulfanyl-N-(4-bromo-3-chloro-phenyl)methanimidothioic acid

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Identification
Molecular formula
C10H9BrClNOS2
CAS number
352553-44-1
IUPAC name
1-allylsulfanyl-N-(4-bromo-3-chloro-phenyl)methanimidothioic acid
State
State

At room temperature, this compound is typically found in a solid state. Its form can range from crystalline to a powdery consistency, depending on how it was synthesized and stored.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
360.67g/mol
Molar mass
360.6700g/mol
Density
1.5600g/cm3
Appearence

1-Allylsulfanyl-N-(4-bromo-3-chloro-phenyl)methanimidothioic acid typically appears as a colorless to pale yellow solid or powder. Its exact appearance can vary depending on the specific sample and purity.

Comment on solubility

Solubility Characteristics of 1-allylsulfanyl-N-(4-bromo-3-chloro-phenyl)methanimidothioic acid

The solubility of 1-allylsulfanyl-N-(4-bromo-3-chloro-phenyl)methanimidothioic acid presents intriguing properties relevant to both its chemical structure and functional groups. Here are some key considerations:

  • Polarity: The compound features a combination of polar and non-polar groups. The presence of an acid functional group (thioic acid) generally enhances solubility in polar solvents like water.
  • Hydrophobic Interactions: However, the alkyl and aromatic groups may introduce significant hydrophobic characteristics, which can reduce solubility in aqueous solutions.
  • Solvent Influence: It is likely to exhibit greater solubility in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), or acetone, due to these non-polar features.

In summary, the solubility of this compound can be categorized as moderately soluble in polar organic solvents while being less soluble in water. It would be essential to consider these factors when working with this compound in various conditions.

Interesting facts

Interesting Facts About 1-Allylsulfanyl-N-(4-bromo-3-chloro-phenyl)methanimidothioic Acid

1-Allylsulfanyl-N-(4-bromo-3-chloro-phenyl)methanimidothioic acid is a fascinating compound that combines various functional groups, showcasing the complexity and versatility of organic chemistry. This compound can be characterized by several intriguing aspects:

  • Functional Diversity: It is rich in functional groups, which allows it to participate in a variety of chemical reactions. This opens up potential pathways for synthesis and application in different fields such as pharmaceuticals and agrochemicals.
  • Structure-Activity Relationship: The presence of bromine and chlorine atoms in the benzene ring significantly influences its biological properties. Halides often enhance the reactivity of compounds due to their electronegative nature, which can result in increased biological activity.
  • Potential Applications: Compounds like this one are often studied for their possible applications in drug development. Due to their ability to mimic biological substrates, they may lead to the discovery of new medicinal agents.
  • Thioic Acid Moiety: The thioic acid component in the structure is noteworthy for its ability to form stable thioester derivatives. Such compounds are key intermediates in various metabolic pathways, including fatty acid synthesis and protein modification.
  • Chiral Centers: The molecule features asymmetric centers, making it a candidate for enantioselective synthesis, which is crucial in creating compounds with specified biological activity.

As a chemistry student or a seasoned scientist, exploring compounds like 1-allylsulfanyl-N-(4-bromo-3-chloro-phenyl)methanimidothioic acid not only enhances understanding of molecular interactions but also opens up avenues for innovative research. Remember, in the world of chemistry, every compound has a story waiting to be uncovered!