Skip to main content

2-Chloro-3-nitrosobutane

ADVERTISEMENT
Identification
Molecular formula
C4H8ClNO
CAS number
.
IUPAC name
2-chloro-3-nitroso-butane
State
State

This compound is in a liquid state at room temperature.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
146.00
Boiling point (Kelvin)
419.15
General information
Molecular weight
121.56g/mol
Molar mass
121.5580g/mol
Density
1.0950g/cm3
Appearence

2-Chloro-3-nitrosobutane typically appears as a colorless to pale yellow liquid. The presence of the nitroso group may lend it a pale yellow hue.

Comment on solubility

Solubility of 2-chloro-3-nitroso-butane

2-chloro-3-nitroso-butane, with the chemical formula C4H8ClN2O, exhibits intriguing solubility characteristics influenced by its structural properties. The presence of a chlorine atom and a nitroso group contributes to the compound's polar nature, thereby affecting how it interacts with various solvents. Here’s a closer look at its solubility behavior:

  • Polar solvents: Given that 2-chloro-3-nitroso-butane contains polar functional groups, it is likely to be soluble in polar solvents such as water and alcohols.
  • Non-polar solvents: Conversely, its solubility in non-polar solvents like hexane is expected to be limited due to the lack of significant non-polar character in its structure.
  • Concentration dependency: The degree of solubility may also vary with temperature and concentration, making it crucial to consider these factors during experimentation.

In summary, the solubility of 2-chloro-3-nitroso-butane can be described as moderate in polar solvents and low in non-polar solvents, reinforcing the pivotal role of molecular structure in determining solubility behaviors. Understanding these relationships is essential for practical applications and further research.

Interesting facts

Interesting Facts about 2-Chloro-3-nitroso-butane

2-Chloro-3-nitroso-butane is a fascinating compound that showcases the interplay between halogenation and nitrosation reactions. Here are some intriguing insights about this compound:

  • Reactivity: The presence of both the chlorine atom and the nitroso group significantly influences the reactivity of 2-chloro-3-nitroso-butane. These functional groups can engage in a variety of chemical reactions, making it a valuable intermediate in synthetic organic chemistry.
  • Applications: This compound is particularly useful in the field of pharmaceuticals and agrochemicals. Its unique structure allows it to act in various synthesis pathways, leading to the development of innovative compounds with biologically active properties.
  • Studying Mechanisms: The study of compounds like 2-chloro-3-nitroso-butane provides insights into reaction mechanisms involving nucleophilic substitutions and electrophilic attacks, which are fundamental concepts in organic chemistry.
  • Safety Precautions: Due to the presence of reactive functional groups, safety should always be a priority when handling 2-chloro-3-nitroso-butane. Protective equipment is essential to prevent any hazardous exposures, and it should be stored under appropriate conditions.
  • Research Potential: As researchers continue to explore its properties, 2-chloro-3-nitroso-butane may lead to new discoveries in material science, such as the development of novel polymers or specialty chemicals.

In summary, 2-chloro-3-nitroso-butane is not just another organic compound; it embodies the complex nature of chemistry where small changes in molecular structure can lead to vastly different chemical behavior and applications. As stated by renowned chemist Robert H. Grubbs, "The beauty of chemistry lies in its unpredictability."

Synonyms
2-chloro-3-nitrosobutane
SCHEMBL8854104
SCHEMBL24364167