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1-Nitrosoazepane

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Identification
Molecular formula
C6H12N2O
CAS number
135-11-5
IUPAC name
1-nitrosoazepane
State
State

At room temperature, 1-Nitrosoazepane is in a liquid state. It is generally stable under normal conditions but should be handled with care due to its reactive nitroso group.

Melting point (Celsius)
-14.00
Melting point (Kelvin)
259.15
Boiling point (Celsius)
208.00
Boiling point (Kelvin)
481.15
General information
Molecular weight
128.18g/mol
Molar mass
128.1840g/mol
Density
1.0250g/cm3
Appearence

1-Nitrosoazepane is a colorless liquid. It can also appear as a pale yellow liquid under certain conditions due to impurities. It is a member of the nitroso compounds, which often have a characteristic pungent smell. The liquid is generally clear and without crystalline structure.

Comment on solubility

Solubility of 1-nitrosoazepane

1-nitrosoazepane, with the chemical formula C7H12N2O, exhibits distinct solubility characteristics that are important for its chemical behavior and potential applications. Understanding its solubility is crucial for predicting how this compound interacts within various environments.

Solubility Characteristics:

  • Polar vs. Nonpolar Solvent Solubility: Given the presence of a nitroso group, 1-nitrosoazepane is likely to show higher solubility in polar solvents due to its ability to form hydrogen bonds.
  • Water Solubility: While specific data on the water solubility of 1-nitrosoazepane may be limited, compounds containing nitrogen and oxygen often exhibit moderate to high solubility in water.
  • Organic Solvents: It is expected to be soluble in common organic solvents such as ethanol and acetone, enhancing its integration into organic reaction systems.

In practice, the solubility of 1-nitrosoazepane can be summarized as follows:

  • Higher solubility in polar solvents
  • Potentially moderate solubility in water
  • Good solubility in organic solvents

As with many chemical compounds, factors such as temperature, pressure, and specific molecular interactions will also influence solubility. Understanding these factors is vital for chemists working with this compound in synthesis and applications.

Interesting facts

Interesting Facts about 1-Nitrosoazepane

1-Nitrosoazepane is a fascinating compound that belongs to the family of nitrosoamines, which are known for their intriguing chemical properties and potential biological activities. Here are some interesting insights about this compound:

  • Structure and Stability: 1-Nitrosoazepane contains a seven-membered ring structure known as azepane, which adds to its unique properties. The incorporation of a nitroso group creates interesting reactivity patterns, making this compound a subject of research for chemists interested in nitrogen-containing compounds.
  • Biological Implications: Some nitrosoamines are known to exhibit carcinogenic properties, raising questions about the safety and handling of compounds like 1-nitrosoazepane in industrial and laboratory settings. It's essential to approach this compound with an understanding of its potential hazards.
  • Reaction Chemistry: 1-Nitrosoazepane could participate in various reactions, including electrophilic substitutions and rearrangements, which make it an attractive substrate in synthetic organic chemistry. This allows chemists to explore innovative synthetic pathways.
  • Applications in Research: The study of 1-nitrosoazepane may contribute to the larger field of medicinal chemistry, particularly in the development of new drugs or the modification of existing pharmaceuticals.
  • Historical Context: The synthesis and study of nitroso compounds date back to the early 20th century, and 1-nitrosoazepane serves as a reminder of the evolving nature of organic chemistry research and the continuous discovery of new compound functionality.

As chemists dive deeper into the world of 1-nitrosoazepane, they uncover not only its chemical behavior but also its potential roles in various chemical contexts. Continued investigation could lead to exciting developments in both practical applications and theoretical understanding!

Synonyms
N-Nitrosohexamethyleneimine
1-Nitrosoazepane
932-83-2
N-Nitrosoperhydroazepine
Nitrosohexamethylenimine
N-Nitrosoazacycloheptane
CCRIS 468
EINECS 213-258-6
BRN 1237798
N67X53N3YT
DTXSID0021040
UNII-N67X53N3YT
DTXCID301040
5-20-04-00067 (Beilstein Handbook Reference)
NITROSOHEXAMETHYLENEIMINE, N-
NNitrosoazacycloheptane
NNitrosoperhydroazepine
NNitrosohexahydroazepine
Hexahydro1nitrosoazepine
NNitrosohexamethylenimine
Hexahydro1nitroso1Hazepine
1HAzepine, hexahydro1nitroso
213-258-6
uzmvsvhutoaptd-uhfffaoysa-n
N-Nitrosohexamethylenimine
N-NITROSOHEXAHYDROAZEPINE
Hexahydro-1-nitroso-1H-azepine
1H-Azepine, hexahydro-1-nitroso-
N-6-MI
Hexahydro-1-nitrosoazepine
1-Nitroso-azepane
Hexahydro-1-nitroso-1H-azepine; N-Nitrosoazacycloheptane; N-Nitrosohexahydroazepine; Nitrosohexamethylenimine
CHEMBL165191
SCHEMBL1578024
AAA93283
Tox21_302820
AKOS006271678
NCGC00256532-01
AS-76918
CAS-932-83-2
DB-297636
NS00039541
D93582
EN300-1296525