Skip to main content

tribromo(nitro)methane

ADVERTISEMENT
Identification
Molecular formula
CBr3NO2
CAS number
560-95-2
IUPAC name
tribromo(nitro)methane
State
State

At room temperature, tribromo(nitro)methane is a solid. It has a characteristic pale yellow color and a crystalline structure.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
244.00
Boiling point (Kelvin)
517.15
General information
Molecular weight
296.73g/mol
Molar mass
296.7300g/mol
Density
3.2600g/cm3
Appearence

Tribromo(nitro)methane appears as a pale yellow solid. It is crystalline in nature.

Comment on solubility

Solubility of Tribromo(nitro)methane

Tribromo(nitro)methane, with the chemical formula CBr3NO2, is a fascinating compound with specific solubility characteristics. Its solubility is primarily influenced by the strong intermolecular forces due to the presence of bromine and nitro groups.

Key Points on Solubility:

  • Polarity: The nitro group (–NO2) contributes to the overall polarity of the molecule, which affects solubility in polar solvents.
  • Solvent Compatibility: Tribromo(nitro)methane is typically soluble in polar organic solvents such as acetone or methanol, while its solubility in nonpolar solvents is significantly reduced.
  • Temperature Effects: Like many chemical compounds, its solubility can vary with temperature; generally, as temperature increases, solubility may also increase.
  • Environmental Considerations: Due to its brominated components, careful consideration must be given to its environmental impact during solubility studies and applications.

In summary, the solubility of tribromo(nitro)methane is dictated by its unique chemical structure, which warrants a nuanced approach when handling or utilizing the compound. As with many halogenated compounds, understanding its solubility is essential for predicting its behavior in various environments and applications.

Interesting facts

Interesting Facts about Tribromo(nitro)methane

Tribromo(nitro)methane, also known as bromoform, is a fascinating organic compound with several noteworthy attributes:

  • Halogenated Compound: This compound is part of a class known as halogenated hydrocarbons, characterized by the presence of bromine atoms. The three bromine atoms in its structure make it highly reactive and unique.
  • Use in Organic Synthesis: Tribromo(nitro)methane is often utilized in organic synthesis reactions, particularly in the synthesis of other complex compounds. Its ability to introduce bromine into various substrates is particularly valuable in the development of pharmaceuticals and agrochemicals.
  • Environmental Impact: As with many organobromine compounds, tribromo(nitro)methane poses environmental and health risks. Its use is monitored due to potential toxicity and its role as a persistent organic pollutant.
  • Biological Studies: Research has shown that tribromo(nitro)methane can affect biological systems; it has been studied for its potential implications in inflammation and cellular response, making it a compound of interest in biochemistry.
  • Regulatory Considerations: Countries have various regulations regarding the use of this compound due to its potential hazards. Understanding its properties is crucial for compliance with environmental safety standards.

Key Takeaways

To summarize, tribromo(nitro)methane is not just another chemical; it's a compound that bridges various fields, from synthetic chemistry to environmental science. Its distinctive properties and implications make it a subject of study for both chemists and environmentalists alike.

"In chemistry, the most common compounds often have the most extraordinary stories." – Unknown

Synonyms
Tribromonitromethane
Bromopicrin
464-10-8
Methane, tribromonitro-
Nitrobromoform
Nitrotribromomethane
CCRIS 5977
Methane, nitrotribromo-
EINECS 207-348-4
BRN 1756139
3412AKG60Q
DTXSID8021511
Methane, nitrotribromo
Methane, tribromonitro
DTXCID801511
207-348-4
tribromo(nitro)methane
Brompikrin
UNII-3412AKG60Q
Bromopicrin (tribromonitromethane)
Bromopicrin;Nitrobromoform
SCHEMBL1775867
ALBB-035673
AKOS040758148
AKOS040766801
FT28398
DB-321793
HY-133635
CS-0128461
NS00007726
Q4912402