2-[N-(4-bromo-3-chloro-phenyl)-C-sulfanyl-carbonimidoyl]sulfanylacetic acid

Identification

Molecular formula

C₉H₇BrClN₂OS₂

CAS number

IUPAC name

2-[N-(4-bromo-3-chloro-phenyl)-C-sulfanyl-carbonimidoyl]sulfanylacetic acid

State

At room temperature, 2-[N-(4-bromo-3-chloro-phenyl)-C-sulfanyl-carbonimidoyl]sulfanylacetic acid is typically a solid.

Melting point (Celsius)

218.00

Melting point (Kelvin)

491.15

Boiling point (Celsius)

488.00

Boiling point (Kelvin)

761.15

General information

Molecular weight

347.61g/mol

Molar mass

347.6140g/mol

Density

1.9330g/cm³

Appearence

The compound appears as a crystalline solid with a distinct coloration due to the presence of bromine and chlorine atoms in its molecular structure. The specific color can range from colorless to pale yellow or light brown depending on the purity and specific formulation of the compound.

Comment on solubility

Solubility of 2-[N-(4-bromo-3-chloro-phenyl)-C-sulfanyl-carbonimidoyl]sulfanylacetic acid

The solubility of 2-[N-(4-bromo-3-chloro-phenyl)-C-sulfanyl-carbonimidoyl]sulfanylacetic acid can be influenced by several factors, including its chemical structure and interactions with solvents. Here are some key points to consider:

Polar Character: The presence of multiple functional groups, such as sulfanyl (-SH) and imidoyl (^-C(=N)-), contributes to its polar nature, which may enhance solubility in polar solvents like water.
Hydrogen Bonding: This compound can engage in hydrogen bonding due to the -SH and carboxylic acid functional groups, potentially increasing its solubility.
Solvent Compatibility: Solubility might also depend on the choice of solvent. For example, it might dissolve better in organic solvents like DMSO (dimethyl sulfoxide) or ethanol rather than in purely aqueous environments.
Temperature Influence: Increased temperatures usually favor the solubility of solid compounds, making it easier for this compound to dissolve under elevated conditions.

In summary, while the specific solubility data for 2-[N-(4-bromo-3-chloro-phenyl)-C-sulfanyl-carbonimidoyl]sulfanylacetic acid may not be readily available, its structural features suggest potential for reasonable solubility in suitable solvents. Understanding its solubility profile is crucial for its applications in various fields of chemistry and pharmacology.

Interesting facts

Interesting Facts about 2-[N-(4-bromo-3-chloro-phenyl)-C-sulfanyl-carbonimidoyl]sulfanylacetic Acid

2-[N-(4-bromo-3-chloro-phenyl)-C-sulfanyl-carbonimidoyl]sulfanylacetic acid is a fascinating compound that highlights the intricate world of organosulfur chemistry. Here are some intriguing points regarding this compound:

Structural Characteristics: This compound features a unique structure consisting of sulfanyl groups which enhances its potential reactivity. The presence of both bromine and chlorine in its phenyl ring exemplifies how halogen substitutions can influence molecular behavior.
Biological Relevance: Compounds containing sulfur are often found in biological systems, playing crucial roles in the function of various biomolecules. They are involved in multiple biological reactions and pathways, underscoring their importance in medicinal chemistry.
Potential Applications: The diverse functionalities of this compound suggest several applications in drug development. Its unique structure may lend itself to properties such as antibacterial or anticancer activities, making it a candidate for further research.
Synthesis Challenges: The synthesis of multi-substituted aromatic compounds like this one often presents challenges. The need for precise control over reaction conditions and purification methods to obtain a pure product is essential, highlighting the complexity of organic synthesis.
Chemical Properties: Sulfur-containing compounds often exhibit interesting properties such as strong odors and distinct reactivity patterns. This compound may engage in various reactions, including nucleophilic substitutions and redox reactions due to the presence of the sulfur atom.
Research Opportunities: With the ongoing advancements in medicinal chemistry, studying such compounds can lead to discovering new pharmaceutical agents. Researchers are always on the lookout for novel chemical entities, and this compound could very well fit that criteria.

In conclusion, 2-[N-(4-bromo-3-chloro-phenyl)-C-sulfanyl-carbonimidoyl]sulfanylacetic acid is an excellent example of how organic compounds can intrigue chemists with their complex structures and potential applications. Its unique characteristics pave the way for further exploration and study.