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2-nitrosonaphthalene

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Identification
Molecular formula
C10H7NO
CAS number
605-87-8
IUPAC name
2-nitrosonaphthalene
State
State

Solid at room temperature, typically in the form of crystalline powder.

Melting point (Celsius)
69.00
Melting point (Kelvin)
342.00
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.00
General information
Molecular weight
157.17g/mol
Molar mass
157.1660g/mol
Density
1.2180g/cm3
Appearence

2-Nitrosonaphthalene typically appears as a pale yellow crystalline solid. It is less commonly encountered compared to other similar compounds, but it has a distinctive color that assists in its identification.

Comment on solubility

Solubility of 2-nitrosonaphthalene

2-nitrosonaphthalene, with the chemical formula C10H7NO2, exhibits unique solubility characteristics that make it a fascinating compound to study. The solubility of this aromatic nitro compound is influenced by several factors:

  • Polarity: 2-nitrosonaphthalene is relatively nonpolar due to its aromatic structure, which generally leads to lower solubility in polar solvents.
  • Solvent Interaction: This compound is more soluble in organic solvents, such as ethyl acetate or chloroform, rather than in water. This is largely because polar solvents struggle to disrupt the aromatic interactions present within the molecule.
  • Temperature Dependency: An increase in temperature often enhances the solubility of organic compounds in nonpolar solvents, making it easier for 2-nitrosonaphthalene to dissolve under elevated conditions.

In summary, when examining the solubility of 2-nitrosonaphthalene, it is essential to consider the following:

  1. Soluble in nonpolar solvents
  2. Poorly soluble in polar solvents
  3. Influenced by temperature

Thus, understanding these solubility properties is crucial for effective applications in chemical synthesis and various industrial processes.

Interesting facts

Interesting Facts about 2-Nitrosonaphthalene

2-Nitrosonaphthalene is an intriguing compound that has captured the attention of scientists and researchers alike. It belongs to the family of nitro aromatic compounds and is recognized for its unique properties and applications. Here are some interesting aspects of this compound:

  • Electrophilic Aromatic Substitution: 2-Nitrosonaphthalene is characterized by its nitro group, which can significantly enhance its reactivity in electrophilic aromatic substitution reactions, making it valuable in synthetic organic chemistry.
  • Biological Activity: Research has indicated that compounds containing the nitroso group can exhibit significant biological activities, such as antibacterial and anticancer properties, leading to potential uses in pharmaceuticals.
  • Environmental Impact: As a byproduct of industrial processes, 2-nitrosonaphthalene can be found in pollution and may pose environmental challenges due to its toxicity and persistence in ecosystems.
  • Research Applications: This compound serves as a subject in various fields of study, including material science, where it's used in the development of new polymers and organic materials.

In the words of renowned chemists, “The exploration of nitro compounds opens doors to a plethora of chemical reactions that are fundamental to the evolution of organic chemistry.” This sentiment reflects the significance of understanding 2-nitrosonaphthalene not merely as a compound, but as a gateway to discovering new chemical processes and potential applications.

Studying 2-nitrosonaphthalene aids in expanding the knowledge within organic chemistry and highlights the importance of nitro compounds in both industrial and environmental contexts. With ongoing research, this compound is likely to reveal even more surprising properties and uses in the future.

Synonyms
2-Nitrosonaphthalene
NAPHTHALENE, 2-NITROSO-
CCRIS 474
3S700W3KWH
BRN 2205947
UNII-3S700W3KWH
NITROSONAPHTHALENE, 2-
DTXSID40216300
DTXCID00138791
6610-08-8
SCHEMBL941460
AKOS006278457
Q27257968