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3H-Imidazo[4,5-c]pyridine

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Identification
Molecular formula
C6H5N3
CAS number
272-97-5
IUPAC name
3H-imidazo[4,5-c]pyridine
State
State

At room temperature, 3H-Imidazo[4,5-c]pyridine exists in a solid state.

Melting point (Celsius)
181.00
Melting point (Kelvin)
454.15
Boiling point (Celsius)
429.00
Boiling point (Kelvin)
702.15
General information
Molecular weight
119.13g/mol
Molar mass
119.1260g/mol
Density
1.3100g/cm3
Appearence

3H-Imidazo[4,5-c]pyridine appears as a solid crystalline compound. It may be off-white to pale brown in color depending on its purity and the specific batch conditions.

Comment on solubility

Solubility of 3H-imidazo[4,5-c]pyridine

3H-imidazo[4,5-c]pyridine, a bicyclic compound, exhibits intriguing solubility properties that are influenced by its structural characteristics. Understanding the solubility of this compound can provide insights into its potential applications, particularly in medicinal chemistry and materials science.

Here are some key points to consider regarding its solubility:

  • Polarity: The presence of nitrogen atoms in the aromatic rings contributes to the polarity of 3H-imidazo[4,5-c]pyridine, which typically enhances its solubility in polar solvents.
  • Solvent Compatibility: It is generally more soluble in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol compared to water.
  • Hydrophobic Interactions: The hydrophobic character of the compound can limit its solubility in highly polar solvents, which is a common behavior among many heterocyclic compounds.
  • Temperature Effects: Solubility may increase with temperature; thus, heating the solvent could enhance the dissolution of 3H-imidazo[4,5-c]pyridine.

In summary, the solubility of 3H-imidazo[4,5-c]pyridine is a complex interplay of polarity, solvent type, and environmental conditions. Understanding these factors is essential for optimizing its use in various chemical applications.

Interesting facts

Exploring 3H-Imidazo[4,5-c]pyridine

3H-Imidazo[4,5-c]pyridine is a fascinating heterocyclic compound that belongs to the class of imidazoles, specifically known for its incorporation of nitrogen atoms into its ring structure. This compound is of significant interest in both organic chemistry and medicinal chemistry due to its intriguing properties and applications.

Key Features:

  • Structural Uniqueness: The fused ring system contains two nitrogen atoms, which contribute to its aromatic character and stability.
  • Biological Significance: This compound exhibits various pharmacological effects, making it a potential candidate in drug discovery and development.
  • Versatile Reactivity: 3H-Imidazo[4,5-c]pyridine can undergo a wide range of chemical reactions, allowing chemists to modify its structure for specific applications.

Researchers are particularly intrigued by the compound's role in:

  • Pharmaceuticals: Many derivatives of 3H-Imidazo[4,5-c]pyridine have been investigated for their biological activities, including anticancer and antitumor properties.
  • Catalysis: It serves as a structural motif in the design of catalysts, facilitating various organic transformations.
  • Material Science: Its unique electronic properties are being explored for potential applications in organic electronics.

As the chemist Richard Feynman once said, "What I cannot create, I do not understand." This perfectly encapsulates the spirit of exploring compounds like 3H-Imidazo[4,5-c]pyridine, where understanding and innovation go hand in hand.

In conclusion, 3H-Imidazo[4,5-c]pyridine stands out not just for its chemical structure but for its broad range of applications and implications in various scientific fields. Its study opens doors to new discoveries and advancements in chemistry, driving the quest for novel compounds that can change the world!

Synonyms
3H-Imidazo[4,5-c]pyridine
5-Azabenzimidazole
272-97-9
1H-Imidazo[4,5-c]pyridine
170245-15-5
1H-Imidazo(4,5-c)pyridine
3,5-DIAZAINDOLE
C6H5N3
imidazo[4,5-c]pyridine
MFCD00051808
imidazo(4,5-c]pyridine
5H-IMIDAZO[4,5-C]PYRIDINE
5-Aza-benzimidazole
NSC521774
imidazo[4,5-c]pyridin
1H-Imidazo4,5-cpyridine
5-Azabenzimidazole, 97%
1H-imidazo[4,5-c]pyridin
SCHEMBL67119
3H-imidazolo[4,5-c]pyridine
CHEMBL286232
SCHEMBL1927520
DTXSID60181667
ALBB-037848
3H-Imidazo[4 pound not5-c]pyridine
CL3548
AKOS005207257
AKOS009158089
CS-W005266
HY-W005266
NSC 521774
NSC-521774
PB20239
AS-20058
PD210465
SY021418
NS00010765
EN300-88369
F2113-0260
Z1117890443
625-811-2