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Bipyridinium dioxime dibromide

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Identification
Molecular formula
C12H14N4O2Br2
CAS number
21276-72-6
IUPAC name
1-[3-[4-(hydroxyiminomethyl)pyridin-1-ium-1-yl]propyl]pyridin-1-ium-4-carbaldehyde oxime;dibromide
State
State

At room temperature, Bipyridinium dioxime dibromide is a solid.

Melting point (Celsius)
238.00
Melting point (Kelvin)
511.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
399.11g/mol
Molar mass
399.1110g/mol
Density
2.8000g/cm3
Appearence

Bipyridinium dioxime dibromide typically appears as a crystalline solid. It is usually colorless to pale yellow in coloration.

Comment on solubility

Solubility of 1-[3-[4-(hydroxyiminomethyl)pyridin-1-ium-1-yl]propyl]pyridin-1-ium-4-carbaldehyde oxime;dibromide

The solubility of the compound 1-[3-[4-(hydroxyiminomethyl)pyridin-1-ium-1-yl]propyl]pyridin-1-ium-4-carbaldehyde oxime;dibromide (C12H14N4O2Br2) is influenced by its unique structural characteristics.

Factors Influencing Solubility:

  • Ionization: Being a quaternary ammonium compound, it is likely to ionize in aqueous solutions, enhancing solubility.
  • Hydrophilicity: The presence of the hydroxyimino group contributes to the polar characteristics of the molecule.
  • Br^- Ions: The dibromide component may also improve solubility by providing additional ionic interactions.

In general:

  • This compound may show good solubility in polar solvents such as water and methanol.
  • However, its solubility in non-polar solvents might be limited due to its ionic nature.

As a result, it's reasonable to state that solubility behavior can vary significantly depending on the solvent system employed. It is advisable to conduct empirical tests to determine the precise solubility profile for specific applications.

Interesting facts

Interesting Facts about 1-[3-[4-(hydroxyiminomethyl)pyridin-1-ium-1-yl]propyl]pyridin-1-ium-4-carbaldehyde oxime; dibromide

This intriguing compound is a fascinating example of the synthesis of complex organic molecules, showcasing several diverse functional groups. Here are a few noteworthy aspects:

  • Structural Complexity: The compound includes multiple pyridine rings, which contribute to its aromatic character and potentially influence its reactivity.
    Pyidine-based structures are often associated with biological activity and have applications in medicinal chemistry.
  • Oxime Functional Group: The presence of the oxime functional group is significant. This group is notable for its ability to participate in various chemical reactions, including rearrangements and condensation reactions, making it a valuable motif in organic synthesis.
  • Biological Relevance: Compounds of similar structure are studied for their pharmacological potential. The pyridine and oxime functionalities can play critical roles in drug design, as they may interact with biological targets.
  • Halogen Influence: The dibromide part of the compound suggests a halogen influence, which can enhance the compound's reactivity and stability. Brominated compounds are known to exhibit a range of properties, including antimicrobial activity.
  • Application Potential: The structural features of this compound may make it an interesting candidate for research in fields such as materials science or as a potential ligand in coordination chemistry.

In summary, 1-[3-[4-(hydroxyiminomethyl)pyridin-1-ium-1-yl]propyl]pyridin-1-ium-4-carbaldehyde oxime; dibromide exemplifies the intricacies of chemical design and its implications for potential applications, particularly in medicinal chemistry and materials science. Its rich structure invites further exploration and emphasizes the creativity inherent in the field of chemistry.

Synonyms
DTXSID101036063
NS00041185
Trimethylen-bis-(pyridinium-4-aldoxim)-dibromid
oxo-[[1-[3-[4-(oxoazaniumylmethylidene)pyridin-1-yl]propyl]pyridin-4-ylidene]methyl]azanium,dibromide