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N-(4-bromophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

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Identification
Molecular formula
C15H11BrClNS2
CAS number
123456-78-9
IUPAC name
N-(4-bromophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid
State
State

The compound is in a solid state at room temperature. It is stable under normal conditions but should be handled with care to avoid exposure to moisture, which may affect its structural integrity.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.15
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.15
General information
Molecular weight
358.58g/mol
Molar mass
358.5810g/mol
Density
1.5600g/cm3
Appearence

The compound is typically found as a yellow crystalline powder. Its appearance may vary slightly depending on the purity and particle size, but it is generally uniform in texture.

Comment on solubility

Solubility of N-(4-bromophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

N-(4-bromophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid is a fascinating compound when it comes to its solubility characteristics. Its solubility can be influenced by various factors including temperature, pH, and the presence of other ions in solution. Here are some key points regarding its solubility:

  • Polarity: The presence of halogen atoms and sulfur groups typically introduces polar characteristics to the compound, which may lead to variances in solubility in polar versus nonpolar solvents.
  • Solvent Interaction: This compound is more likely to dissolve in polar solvents such as water, ethanol, and dimethyl sulfoxide (DMSO) due to hydrogen bonding and dipole interactions.
  • Temperature Effects: Increased temperature generally enhances the solubility of solids in liquids; thus, heating may significantly improve the dissolution rate of this compound.
  • pH Sensitivity: The acidic nature of the thioic acid group can lead to increased solubility in alkaline conditions due to deprotonation, which increases the compound’s ionic character.

It's worth noting that "the solubility of any compound is a critical property that dictates its utility in various applications." Understanding the solubility profile of N-(4-bromophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid can lead to better insights when it comes to environmental behavior, bioavailability, and potential chemical reactivity.

Interesting facts

Interesting Facts about N-(4-bromophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

N-(4-bromophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid is a complex organic compound that showcases the fascinating interplay of halogenated phenyl groups and thioamide functionality. Here are some notable aspects of this remarkable compound:

  • Structural Complexity: The presence of both a bromine and a chlorine substituent on the phenyl rings contributes to the compound’s chemical reactivity and possible interactions with biological systems. This diversity adds an interesting level of complexity for chemists studying structure-activity relationships.
  • Potential Applications: Compounds with similar structural motifs have been investigated for various applications such as pharmaceuticals, agrochemicals, and dendritic materials due to their unique properties. The specific substitution pattern may suggest potential herbicidal or antibacterial activities.
  • Synthetic Pathways: The synthesis of this compound may involve multiple steps, including the introduction of halogens and the formation of thioamide. Understanding these synthesis routes aids in the development of more efficient methods for producing such compounds.
  • Thioic Acid Group: The thioic acid moiety (−C(=S)−SH) is of considerable interest in organic chemistry and biochemistry as it can participate in diverse reactions, including nucleophilic attacks and coordination with metals.
  • Scientific Interest: Compounds featuring substituted phenyl groups are often studied for their *electronic and steric effects*. Understanding these interactions can provide valuable insights into reaction mechanisms and the development of new materials.

As with many compounds featuring halogen substituents, the study of N-(4-bromophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid may also reveal important information about environmental persistence and toxicity, which are critical factors in modern chemical research.

In conclusion, this compound serves not just as a chemical entity but also as a portal to explore broader concepts in organic synthesis, reactivity, and potential biological implications. The journey into its study can illuminate various pathways in both academic and practical applications.