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2-(4-Nitrophenyl)selanylacetic acid

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Identification
Molecular formula
C8H7NO4Se
CAS number
70086-39-4
IUPAC name
2-(4-nitrophenyl)selanylacetic acid
State
State

At room temperature, 2-(4-Nitrophenyl)selanylacetic acid is in a solid state. Its crystalline nature makes it easy to handle in a laboratory setting for organic synthesis or study of selenium-containing compounds.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.15
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.15
General information
Molecular weight
291.11g/mol
Molar mass
291.1410g/mol
Density
1.6390g/cm3
Appearence

2-(4-Nitrophenyl)selanylacetic acid appears as a yellow to orange crystalline solid. The color intensity can vary depending on the specific sample and its purity. The compound is stable under normal conditions but should be stored away from light and moisture to prevent degradation.

Comment on solubility

Solubility of 2-(4-nitrophenyl)selanylacetic acid

The solubility of 2-(4-nitrophenyl)selanylacetic acid, a compound distinguished by its unique selenol functional group, can exhibit noteworthy characteristics that depend on various factors. Understanding its solubility is crucial for applications in medicinal chemistry and materials science. Here are some key points to consider:

  • Polar vs. Nonpolar: The presence of both the nitrophenyl group and the selenylacetic acid moiety suggests that this compound may present a balance between polar and nonpolar characteristics, which could influence its solubility in different solvents.
  • Solvent Properties: 2-(4-nitrophenyl)selanylacetic acid is likely to be more soluble in polar solvents such as water or alcohols due to the ability of the acid group to stabilize solvation through hydrogen bonding.
  • pH Dependence: The solubility of acidic compounds can be affected by pH levels. In more alkaline conditions, the acid may deprotonate, potentially increasing solubility due to the formation of anions.
  • Crystallization Behavior: As a uniquely structured compound, its solubility can also be impacted by factors like temperature, which might promote or hinder crystallization during synthesis or storage.

In summary, while specifics about the solubility of 2-(4-nitrophenyl)selanylacetic acid in various solvents may vary, its potential behavior underscores the importance of examining solvent compatibility, pH levels, and environmental conditions for optimal usage in chemical applications.

Interesting facts

Interesting Facts about 2-(4-nitrophenyl)selanylacetic acid

2-(4-nitrophenyl)selanylacetic acid is a unique organoselenium compound that combines the properties of both selenium and an aromatic nitro group, making it a subject of interest in various scientific fields, particularly in medicinal chemistry and materials science. Here are some intriguing aspects:

  • Organoselenium Chemistry: Selenium is known for its versatile chemistry, especially in the formation of organoselenium compounds. These compounds exhibit a wide range of biological activities, including antioxidant properties, which can be essential for developing pharmaceuticals.
  • Applications in Medicine: The presence of the nitrophenyl group can enhance the biological activity of the compound. Such modifications can lead to promising candidates for drug development, potentially targeting various diseases, including cancer.
  • Reactivity and Coordination: The selenium atom in this compound demonstrates unique reactivity patterns. It can participate in coordination chemistry, which may be useful for creating new materials with interesting electronic properties.
  • Research Potential: Ongoing studies are investigating the use of organoselenium compounds in organic synthesis and as potential agents in agricultural chemistry, showcasing their importance in both health and environmental contexts.
  • Exploration of Selenoacetic Acid: The acetic acid part of the molecule suggests potential applications as a building block in various organic syntheses, expanding its utility in synthesizing more complex structures.

In summary, 2-(4-nitrophenyl)selanylacetic acid stands out not only for its structural composition but also for its potential applications across multiple disciplines. Its reactivity and biological significance continue to inspire chemists and researchers around the globe.

Synonyms
17893-55-9
(p-Nitrophenylselenyl)acetic acid
ACETIC ACID, (p-NITROPHENYLSELENYL)-
BRN 2270000
DTXSID00170616
2-06-00-00322 (Beilstein Handbook Reference)
DTXCID3093107
2-(4-nitrophenyl)selanylacetic acid
[(p-Nitrophenyl)seleno]acetic acid
acetic acid, 2-(4-nitrophenyl)seleno-