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4-bromo-1,2-dimethyl-5-nitroimidazole

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Identification
Molecular formula
C5H6BrN3O2
CAS number
56322-54-4
IUPAC name
4-bromo-1,2-dimethyl-5-nitro-imidazole
State
State

At room temperature, this compound is found in a solid state. It is stable under normal laboratory conditions but should be stored in a cool, dry place, away from any sources of ignition or incompatible materials.

Melting point (Celsius)
121.50
Melting point (Kelvin)
394.65
Boiling point (Celsius)
312.00
Boiling point (Kelvin)
585.15
General information
Molecular weight
235.02g/mol
Molar mass
235.0390g/mol
Density
1.7100g/cm3
Appearence

4-Bromo-1,2-dimethyl-5-nitroimidazole is typically a yellow crystalline solid. Its distinct coloration is due to the presence of the nitro group, which imparts a yellow hue. The crystals are often well-formed and can be handled with standard laboratory procedures, although care should be taken due to their chemical nature.

Comment on solubility

Solubility of 4-bromo-1,2-dimethyl-5-nitro-imidazole

The solubility of 4-bromo-1,2-dimethyl-5-nitro-imidazole is influenced by several factors due to its complex molecular structure. This compound, which contains both bromine and nitro functional groups, exhibits interesting potential for solubility behavior in various solvents.

  • Polar Solvents: This imidazole derivative is expected to have moderate solubility in polar solvents such as water or alcohols, as the presence of the nitro group may enhance polarity.
  • Non-Polar Solvents: Solubility in non-polar solvents may be limited due to the overall polarity of the molecule. The bromine and dimethyl groups could contribute to some level of non-polar interactions.
  • pH Influence: The solubility may also be affected by pH, given the presence of nitrogen atoms that can be protonated or deprotonated depending on the conditions, potentially leading to increased solubility in acidic or basic environments.

In conclusion, while the general trend suggests that 4-bromo-1,2-dimethyl-5-nitro-imidazole may show reasonable solubility in polar solvents, its solubility characteristics can vary markedly. Understanding the solubility of this compound is essential for applications in pharmaceuticals and chemical synthesis, making it a topic worthy of further investigation.

Interesting facts

Interesting Facts about 4-Bromo-1,2-dimethyl-5-nitro-imidazole

4-Bromo-1,2-dimethyl-5-nitro-imidazole is a fascinating compound that belongs to the imidazole family, characterized by its unique structure and chemical properties. Here are some intriguing insights:

  • Versatile Applications: This compound has been explored for its potential use in pharmaceuticals, particularly as an antibacterial agent. Its imidazole ring is a common scaffold in drug design.
  • Structural Diversity: The introduction of bromo and nitro groups on the imidazole ring adds to the compound's reactivity, making it a valuable intermediate in organic synthesis.
  • Biological Significance: Imidazole derivatives have been noted for their biological activity, including antifungal, antiviral, and anticancer properties, making them significant in medicinal chemistry.
  • Research Interest: Scientists are actively studying compounds like this, as the presence of multiple substituents can lead to varied pharmacological effects, opening doors for new therapeutic agents.

In summary, 4-bromo-1,2-dimethyl-5-nitro-imidazole is much more than just a chemical entity; it represents a critical area of research in medicinal chemistry, illustrating the importance of structure-activity relationships in drug development. As one researcher aptly said, "Chemistry is about connections and creating pathways to new possibilities."

Synonyms
21431-58-3
4-BROMO-1,2-DIMETHYL-5-NITROIMIDAZOLE
Imidazole, 4-bromo-1,2-dimethyl-5-nitro-
DTXSID60175703
RefChem:348871
DTXCID4098194
4-Bromo-1,2-dimethyl-5-nitro-1H-imidazole
starbld0031695
CHEMBL289285
SCHEMBL8345199
ZNTMHCHYIKJJMI-UHFFFAOYSA-N
EN300-54555
4-Bromo-1,2-dimethyl-5-nitro-1H-imidazole #