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EZIPT

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Identification
Molecular formula
C11H13Cl2N3O2
CAS number
25976-17-6
IUPAC name
1H-imidazole-1,3-diium-4-ylmethyl pyridine-4-carboxylate;dichloride
State
State

Under standard conditions, the compound exists as a solid.

Melting point (Celsius)
203.00
Melting point (Kelvin)
476.15
Boiling point (Celsius)
307.00
Boiling point (Kelvin)
580.15
General information
Molecular weight
283.15g/mol
Molar mass
283.1500g/mol
Density
1.4800g/cm3
Appearence

The compound typically appears as a white crystalline solid.

Comment on solubility

Solubility of 1H-imidazole-1,3-diium-4-ylmethyl pyridine-4-carboxylate; dichloride

The solubility of 1H-imidazole-1,3-diium-4-ylmethyl pyridine-4-carboxylate dichloride is a fascinating subject, especially considering its complex structure. Understanding the solubility of this compound can be broken down into several key factors:

  • Polarity: The presence of both imidazole and pyridine functional groups suggests that the compound is polar. This polarity can enhance its solubility in polar solvents, such as water, due to favorable interactions.
  • Salt Form: As a dichloride, this compound likely exists as a salt. Salts generally tend to have higher solubility in aqueous solutions compared to their non-salt counterparts.
  • Hydrogen Bonding: The nitrogen atoms in the imidazole and pyridine rings can engage in hydrogen bonding with water molecules, promoting solubility.

While specific solubility data may vary depending on environmental conditions, such as temperature and pH, it is often observed that:

  • Many imidazole derivatives have a high tendency to dissolve in water.
  • Salt forms of pyridine derivatives are typically more soluble than their neutral forms due to ion-dipole interactions.

In conclusion, while precise solubility values for 1H-imidazole-1,3-diium-4-ylmethyl pyridine-4-carboxylate dichloride may require experimental data, its structural characteristics suggest that it would exhibit good solubility in polar solvents, primarily due to the presence of polar functional groups and the ionic nature of the salt form.

Interesting facts

1H-Imidazole-1,3-diium-4-ylmethyl pyridine-4-carboxylate; dichloride

1H-Imidazole-1,3-diium-4-ylmethyl pyridine-4-carboxylate; dichloride is a fascinating compound characterized by its involvement in various biochemical processes and potential applications. Here are some noteworthy facts about this unique compound:

  • Structural Significance: The compound features an imidazole ring, a structure prevalent in many biological molecules, particularly amino acids and nucleotides, which underlines its biochemical relevance.
  • Protonation Characteristics: The presence of the imidazole moiety contributes to the compound's capacity to act as a proton donor or acceptor, making it a versatile participant in acid-base chemistry.
  • Pharmacological Potential: Compounds similar to this one may target specific receptors in the body. In particular, derivatives of imidazole are often studied for their potential to act as anti-inflammatory and anti-cancer agents.
  • Coordination Chemistry: The dichloride aspect suggests that this compound can engage in coordination with metal ions, a property that could be exploited in catalysis or for the development of new materials.
  • Research Applications: This compound's structural diversity indicates its potential uses in various fields such as medicinal chemistry, materials science, and nanotechnology.
  • Chemical Relativity: The molecular framework of this compound indicates how small changes in functional groups can lead to significantly different chemical behaviors, underscoring the intricate nature of chemical reactivity.

Overall, the exploration of 1H-imidazole-1,3-diium-4-ylmethyl pyridine-4-carboxylate; dichloride exemplifies the rich interplay between structure and function in chemistry. As researchers continue to investigate this compound, we may uncover even more of its potential applications and properties that could benefit both science and industry.

Synonyms
ISONICOTINIC ACID, IMIDAZOL-4-YLMETHYL ESTER, DIHYDROCHLORIDE
20062-43-5
Imidazole-4-methanol, isonicotinate (ester), dihydrochloride