N-(2-nitrosocyclohexen-1-yl)hydroxylamine

Identification

Molecular formula

C₆H₈N₂O

CAS number

126-11-4

IUPAC name

N-(2-nitrosocyclohexen-1-yl)hydroxylamine

State

At room temperature, it is a solid.

Melting point (Celsius)

60.50

Melting point (Kelvin)

333.65

Boiling point (Celsius)

161.00

Boiling point (Kelvin)

434.00

General information

Molecular weight

128.15g/mol

Molar mass

128.1500g/mol

Density

1.3800g/cm³

Appearence

This compound typically appears as a yellow crystalline solid.

Comment on solubility

Solubility of N-(2-nitrosocyclohexen-1-yl)hydroxylamine

N-(2-nitrosocyclohexen-1-yl)hydroxylamine is a compound that exhibits interesting solubility characteristics, influenced by its molecular structure and functional groups. Here are key points regarding its solubility:

Solvent Interaction: This compound is likely to be soluble in polar solvents due to the presence of hydrophilic functional groups, such as the hydroxylamine moiety.
Water Solubility: Its solubility in water may be moderate; while nitroso and hydroxyl groups can enhance solubility, steric effects from the cyclohexene structure could inhibit complete dissolution.
Organic Solvents: It may show better solubility in organic solvents, such as ethanol or methanol, which can stabilize the molecule through hydrogen bonding.
Temperature Dependence: The solubility might increase with rising temperature, potentially leading to interesting applications in reactions where temperature control is crucial.

In conclusion, understanding the solubility of N-(2-nitrosocyclohexen-1-yl)hydroxylamine is pivotal for dictating its use in various chemical applications, as solubility affects reactivity, bioavailability, and overall performance in chemical processes.

Interesting facts

Interesting Facts about N-(2-nitrosocyclohexen-1-yl)hydroxylamine

N-(2-nitrosocyclohexen-1-yl)hydroxylamine is a fascinating chemical compound that has captured the attention of chemists due to its unique structural and reactive properties. Here are some interesting aspects of this compound:

Nitrosation: This compound is an example of a nitrosamine, which is often formed by the reaction of amines with nitrous acid. Nitrosamines are significant in both organic chemistry and biochemistry due to their roles in various biological processes.
Functional Versatility: The compound features a hydroxylamine functional group, which is known for its ability to participate in a variety of reactions. Hydroxylamines can be used as reducing agents and play a role in organic synthesis.
Biological Relevance: Though nitrosamines are often associated with carcinogenic properties, not all are harmful. The study of N-(2-nitrosocyclohexen-1-yl)hydroxylamine can provide insight into chemical pathways and the mechanisms of certain biological processes.
Environmental Impact: Understanding the stability and reactivity of nitrosamines is crucial for environmental chemistry, as they can arise from various biological and chemical processes in the environment.
Research and Applications: Ongoing research is focused on the implications of nitrosamines in pharmacology and toxicology. Understanding the derivatives of compounds like N-(2-nitrosocyclohexen-1-yl)hydroxylamine can lead to advancements in drug development and mitigation strategies for toxic substances.

In conclusion, N-(2-nitrosocyclohexen-1-yl)hydroxylamine bridges various fields of chemistry and biology, offering a glimpse into the complexities of functional group reactions and environmental chemistry. As scientists continue to investigate its properties and implications, this compound remains a subject of interest, revealing more about both synthetic pathways and biological interactions.