N'-(4-nitrosophenyl)benzohydrazide;thioarsorosomethane

Identification

Molecular formula

C₁₃H₁₁N₃O₂

IUPAC name

State

At room temperature, N'-(4-nitrosophenyl)benzohydrazide exists in the solid state as crystalline substances, typically protected from light and moisture to ensure stability and prevent degradation.

Thioarsorosomethane, depending on specific chemical configuration and environment, might be found as a liquid.

Melting point (Celsius)

149.00

Melting point (Kelvin)

422.15

Boiling point (Celsius)

290.00

Boiling point (Kelvin)

563.15

General information

Molecular weight

251.23g/mol

Molar mass

251.2340g/mol

Density

1.4503g/cm³

Appearence

N'-(4-nitrosophenyl)benzohydrazide is typically encountered as a solid compound, characterized by its crystalline form. The compound exhibits a distinct color due to the nitroso group, which generally imparts a yellow to greenish hue.

Thioarsorosomethane is a complex organoarsenic compound which may appear as a liquid. The coloration varies, but it may be colorless or slightly yellow, attributable to its chemical structure.

Comment on solubility

Solubility of N'-(4-nitrosophenyl)benzohydrazide; thioarsorosomethane

The solubility characteristics of the compound N'-(4-nitrosophenyl)benzohydrazide; thioarsorosomethane are influenced by its unique chemical structure and functional groups. Understanding its solubility is crucial for various applications in synthesis and analytical chemistry.

Key Points on Solubility:

Polar vs. Non-Polar: N'-(4-nitrosophenyl)benzohydrazide features polar functional groups that can enhance solubility in polar solvents such as water and alcohols.
Hydrophobic Interactions: The presence of aromatic rings may contribute to hydrophobic interactions, potentially limiting solubility in non-polar solvents.
Dependency on Temperature: Solubility can vary with temperature; typically, higher temperatures may improve solvation and enhance the dissolution of solids.
pH Effects: The solubility of this compound may also be influenced by the pH of the solution, as ionization of functional groups can alter solubility properties.

In sum, the solubility of N'-(4-nitrosophenyl)benzohydrazide; thioarsorosomethane is highly dependent on the solvent environment, the temperature, and the pH level. Understanding these properties is essential for successful application in laboratory or industrial settings.

Interesting facts

Interesting Facts about N'-(4-nitrosophenyl)benzohydrazide; thioarsorosomethane

N'-(4-nitrosophenyl)benzohydrazide; thioarsorosomethane is a fascinating compound with intriguing applications and properties that make it a noteworthy subject of study. Here are some interesting highlights:

Dual Functionality: This compound combines the properties of both an aromatic hydrazide and a thioarsorosomethane, suggesting potential applications in pharmaceuticals and agrochemicals.
Reactivity: The presence of the nitroso group (N=O) in N'-(4-nitrosophenyl)benzohydrazide makes it a reactive compound, which may participate in various chemical reactions, such as condensation and diazotization, leading to the synthesis of more complex molecules.
Biological Relevance: Compounds containing nitroso groups have been studied for their biological activity, including possible use as anti-cancer agents or in the treatment of other diseases due to their ability to interact with biological molecules.
Environmental Significance: As thioarsorosomethane features arsenic, the environmental impact of this compound is crucial, especially in regions where arsenic contamination is prevalent. Understanding its behavior and breakdown in the environment is key to developing mitigation strategies.

The study of N'-(4-nitrosophenyl)benzohydrazide; thioarsorosomethane exemplifies how compounds can offer a unique blend of chemical features and real-world implications. Through continued research, scientists may unlock new pathways for innovation in medicine and environmental science, enhancing our understanding of both chemistry and its applications.

Synonyms

AGN-PC-0JKHSW

8066-69-1

DTXSID50274774