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1-nitrosoazepane

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Identification
Molecular formula
C6H12N2O
CAS number
593-79-3
IUPAC name
1-nitrosoazonane
State
State

At room temperature, 1-nitrosoazepane is typically a liquid. It is a mobile fluid that exhibits the physical properties common to light organic liquids.

Melting point (Celsius)
-75.00
Melting point (Kelvin)
198.15
Boiling point (Celsius)
155.00
Boiling point (Kelvin)
428.15
General information
Molecular weight
142.18g/mol
Molar mass
142.2010g/mol
Density
0.9400g/cm3
Appearence

1-Nitrosoazepane typically appears as a colorless to pale yellow liquid. It is mobile and can have an oily texture. This compound may exhibit a mild characteristic odor.

Comment on solubility

Solubility of 1-nitrosoazonane

The solubility of 1-nitrosoazonane can be quite intriguing, given its unique chemical structure. Generally, the solubility of compounds is influenced by several key factors:

  • Polarity: The presence of polar functional groups, such as the nitroso group, can enhance solubility in polar solvents.
  • Hydrogen Bonding: If 1-nitrosoazonane can form hydrogen bonds, it may exhibit increased solubility in water and alcohols.
  • Molecular Size: Larger molecules may show reduced solubility due to steric hindrance.
  • Temperature: Increasing temperature can often boost solubility, allowing more solute to dissolve.

While 1-nitrosoazonane is not as well-studied as some other compounds, early findings suggest that its solubility characteristics may be influenced by the balance of its hydrophobic and hydrophilic portions. As a rule of thumb, "like dissolves like," meaning it is likely soluble in solvents that share similar polarities. However, experimental determination of its solubility range remains crucial for practical applications and further understanding.

Interesting facts

Interesting Facts about 1-nitrosoazonane

1-nitrosoazonane is a fascinating organic compound that falls within the category of nitroso compounds. Here are some intriguing aspects of this compound:

  • Structure & Stability: As a member of the azole compounds, 1-nitrosoazonane contains both a nitrogen-nitrogen bond and a functional nitroso group, which contributes to its unique reactivity. The presence of these functional groups makes the compound interesting for studying the stability of such nitrogen-containing compounds.
  • Reactivity: The nitroso group is known to be electrophilic, allowing it to participate in various chemical reactions, such as nucleophilic substitutions and coupling reactions. This property can be leveraged in synthetic organic chemistry for the formation of complex molecules.
  • Biological Relevance: Some studies suggest that nitroso compounds can exhibit biological activity, potentially leading to implications in medicinal chemistry. Understanding the behavior of 1-nitrosoazonane could open avenues for research into new pharmaceuticals or agricultural chemicals.
  • Analytical Applications: 1-nitrosoazonane can serve as a useful reagent in analytical chemistry, particularly in the determination of certain metals or in spectroscopic studies, adding to its utility beyond just being a compound of interest.
  • Caution: It is important to note that many nitroso compounds, including 1-nitrosoazonane, may pose potential health risks. Proper precautions should always be taken while handling such compounds in the laboratory.

In summary, 1-nitrosoazonane offers a blend of intriguing structure, reactivity, and potential applications, making it a noteworthy subject in the field of chemistry.

Synonyms
N-Nitrosoazacyclononane
1H-AZONINE, OCTAHYDRO-1-NITROSO-
N-Nitrosooctamethyleneimine
Octahydro-1-nitroso-1H-azonine
20917-50-4
BRN 1365390
DTXSID90175074
5-20-04-00204 (Beilstein Handbook Reference)
NNitrosoazacyclononane
Octahydro1nitroso1Hazonine
1HAzonine, octahydro1nitroso
DTXCID7097565
RefChem:438024
1-Nitrosoazonane
1-Nitroso-azonane
1-Nitrosoazonane #
CHEMBL352105
T6DM86PZ77
DTEBJZRWYBQINZ-UHFFFAOYSA-N
NITROSOOCTAMETHYLENIMINE, N-
AKOS006277907