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2-nitroso-1-phenyl-ethenol

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Identification
Molecular formula
C8H7NO2
CAS number
84449-67-6
IUPAC name
2-nitroso-1-phenyl-ethenol
State
State

At room temperature, it is usually found as a solid.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
149.15g/mol
Molar mass
149.1510g/mol
Density
1.2900g/cm3
Appearence

2-Nitroso-1-phenyl-ethenol typically appears as a yellow to orange crystalline powder. The compound is typically stable under recommended storage conditions, protected from moisture and heat.

Comment on solubility

Solubility of 2-nitroso-1-phenyl-ethenol

2-nitroso-1-phenyl-ethenol, with its intriguing structure, presents interesting characteristics regarding its solubility:

  • Polar Nature: The presence of the hydroxyl (-OH) group contributes to its polarity, making it potentially soluble in polar solvents.
  • Solvent Interaction: Generally, it is expected to dissolve more readily in water compared to nonpolar solvents due to hydrogen bonding capabilities.
  • Hydrogen Bonding: The capacity to form hydrogen bonds is crucial as it typically enhances solubility in polar environments, allowing for better solvation.
  • Structural Consideration: The phenyl group introduces some hydrophobic characteristics, which may limit solubility in high-polarity environments.

In summary, while 2-nitroso-1-phenyl-ethenol is likely soluble in polar solvents due to hydrogen bonding, the overall solubility may be influenced by the balance between its polar and nonpolar characteristics. Therefore, the exact solubility may depend on the specific solvent system employed.

Interesting facts

Interesting Facts about 2-Nitroso-1-phenyl-ethenol

2-Nitroso-1-phenyl-ethenol is an intriguing compound that garners interest due to its unique structural components and chemical properties. Here are some noteworthy points to consider:

  • Functional Groups: This compound features a nitroso group (-NO) attached to an enol functional group. This combination makes it a subject of study in understanding various reactivity patterns and stabilization mechanisms in organic chemistry.
  • Isomerism: Its nitrogen-containing group introduces the possibility of several isomeric forms, which can lead to different chemical behaviors and reactions. Isomers are crucial in the study of organic compounds, as they can exhibit vastly different properties despite having the same molecular formula.
  • Applications in Synthesis: 2-Nitroso-1-phenyl-ethenol can serve as a precursor for synthesizing more complex molecules. This is particularly important in pharmaceuticals where building blocks need to be modified to create effective drugs.
  • Analytical Chemistry: The presence of the nitroso functionality provides utility in analytical techniques. The unique spectroscopic properties of this compound can allow for its identification and quantification in various mixtures, making it a valuable tool in research laboratories.
  • Historical Significance: Compounds that contain both nitroso and enol functionalities have a rich history in organic synthesis and have often been involved in studies concerning reaction mechanisms, contributing to our overall understanding of chemical reactivity.

In summary, 2-nitroso-1-phenyl-ethenol is more than just a molecular formula; it embodies a wealth of knowledge and potential in the field of organic chemistry. Its unique characteristics and applications reinforce the importance of studying such compounds for advancements in chemical research.