N-(4-bromo-3-chloro-phenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

Identification

Molecular formula

C₁₄H₁₀BrCl₂NS

CAS number

96927-15-6

IUPAC name

N-(4-bromo-3-chloro-phenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

State

The compound is in a solid state at room temperature. Its crystalline form is typical of many organic compounds containing halogen groups.

Melting point (Celsius)

96.30

Melting point (Kelvin)

369.50

Boiling point (Celsius)

255.70

Boiling point (Kelvin)

528.90

General information

Molecular weight

327.66g/mol

Molar mass

327.6620g/mol

Density

1.5850g/cm³

Appearence

The compound typically appears as a yellow crystalline powder. Its aromatic nature along with bromine and chlorine substitution contributes to this distinct coloration.

Comment on solubility

Solubility of N-(4-bromo-3-chloro-phenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

The solubility of N-(4-bromo-3-chloro-phenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid can be described as follows:

Polar Solvents: This compound is likely to exhibit good solubility in polar solvents such as water and methanol, due to its multiple functional groups that can engage in hydrogen bonding and dipole interactions.
Non-Polar Solvents: On the other hand, solubility in non-polar solvents (e.g., hexane) is expected to be lower, as the significant presence of electronegative atoms may hinder interactions with non-polar environments.
pH Dependence: The acidic group may cause pH-dependent solubility variations. In an acidic medium, the compound could exist predominantly in its protonated form, enhancing solubility.
Temperature Influence: Like many organic compounds, an increase in temperature may improve solubility as kinetic energy facilitates interactions and dissolution processes.

It is important to note that experimental solubility data may be required to fully characterize the solubility behavior of this complex compound in various solvents. As quoted, “The solubility of a compound is often a key indicator of its potential biological activity and applications.” Thus, understanding solubility can not only reveal insight into its chemistry but also inform its practical uses.

Interesting facts

Exploring N-(4-bromo-3-chloro-phenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

N-(4-bromo-3-chloro-phenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid, with its intriguing structure, belongs to the family of thioacids and is known for its unique properties and potential applications in various fields. Here are some fascinating facts about this compound:

Medicinal Applications: Research indicates that compounds containing a thioic acid moiety may exhibit significant biological activity. This derivative could potentially be explored for its antimicrobial and anti-inflammatory properties.
Synthetic Pathways: The synthesis of this compound can involve various methods, including the reaction of thiols with carboxylic acid derivatives. This highlights the versatility of organic synthesis techniques in creating complex molecules.
Structural Features: The presence of multiple halogens (bromine and chlorine) in its structure may enhance the reactivity and stability of this compound, making it an interesting subject of study in organosilicon chemistry.
Environmental Impact: As with many halogenated compounds, understanding the environmental behavior and degradation mechanisms of this substance is crucial for assessing its safety and ecological footprint.

In summary, N-(4-bromo-3-chloro-phenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid serves as a prime example of how synthetic organic chemistry can yield compounds with potential pharmacological and environmental implications. As a chemist delving into this compound, one might ponder the myriad reactions and interactions it could undergo, paving the way for future discoveries.