N-(4-bromo-3-methylphenyl)-1-ethylsulfanyl-methanimidothioic acid

Identification

Molecular formula

C₁₁H₁₂BrNS₂

CAS number

.000

IUPAC name

N-(4-bromo-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid

State

At room temperature, this compound is generally found in a solid-state, often used in its crystalline form for chemical syntheses or reactions in research and industrial applications.

Melting point (Celsius)

152.00

Melting point (Kelvin)

425.15

Boiling point (Celsius)

338.00

Boiling point (Kelvin)

611.15

General information

Molecular weight

305.22g/mol

Molar mass

305.2200g/mol

Density

1.5000g/cm³

Appearence

The compound is typically a solid at room temperature, with crystalline characteristics. It can appear as off-white to pale yellow in color, depending on the purity and specific preparation methods.

Comment on solubility

Solubility Characteristics of N-(4-bromo-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid

N-(4-bromo-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid, a complex organic compound, presents intriguing solubility behavior. Understanding the solubility of this compound is essential for its applications in various fields. Here are some key points to consider:

Polarity: The compound features both polar and nonpolar functional groups, which greatly influences its solubility profile.
Solvents: It is likely to exhibit:

Moderate solubility in polar solvents such as water or alcohols, due to the presence of the acid group.
Higher solubility in organic solvents, like dichloromethane or ethanol, owing to its hydrophobic phenyl and ethyl groups.

Temperature Influence: Generally, the solubility can increase with temperature, enhancing molecular interactions.
pH Effect: The solubility might vary significantly with changes in pH, particularly because of the acid nature which can dissociate in basic conditions.

It is important to conduct experiments to ascertain precise solubility values as these can differ based on concentration and environmental factors. In summary, the solubility of N-(4-bromo-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid is a blend of its unique chemical characteristics, requiring careful consideration for effective use.

Interesting facts

Interesting Facts about N-(4-bromo-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid

N-(4-bromo-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid is a compound of notable interest in the field of synthetic chemistry and medicinal research. Here are some intriguing aspects of this chemical compound:

Structural Complexity: This compound features a unique arrangement of functional groups, which makes it a prime candidate for various applications in organic synthesis.
Brominated Aromatic System: The presence of a bromine atom introduces both reactivity and potential for bioactivity, often enhancing the compound's properties in medicinal chemistry.
Sulfanyl Group: The ethylsulfanyl component is of particular interest due to its role in increasing solubility in organic solvents, which is crucial for pharmaceutical formulations.
Potential Applications: Compounds with similar structures have been studied for their potential as anti-cancer agents, antimicrobial agents, and in the development of pesticides.
Research Opportunities: This compound opens up multiple avenues for research, particularly in exploring the mechanisms of action and potential biological effects.

In conclusion, N-(4-bromo-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid is not only a fascinating compound in terms of its molecular biology but also serves as a valuable tool in chemical research. Its structural features provide insight into how modifications can lead to enhanced activity in various applications.