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No approved common name

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Identification
Molecular formula
C19H12FN4O2
CAS number
. Not assigned
IUPAC name
4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]pyridine
State
State

At room temperature, this compound is typically in a solid state. It is often handled in a pure powder form for research and application processes.

Melting point (Celsius)
154.00
Melting point (Kelvin)
427.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
356.32g/mol
Molar mass
356.3410g/mol
Density
1.4347g/cm3
Appearence

This compound typically appears as a crystalline solid. The color can vary based on purity and any specific structural configuration, but it's often found as a white to off-white solid.

Comment on solubility

Solubility of 4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]pyridine

The solubility characteristics of the compound 4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]pyridine (C19H12FN4O2) are intriguing due to its complex molecular structure. This compound, which comprises both fluorine and nitro groups, exhibits behavior that can be influenced by several factors, including:

  • Polarity: The presence of polar functional groups, such as the nitro group, may enhance solubility in polar solvents.
  • Hydrophobicity: The aromatic rings contribute to a hydrophobic character that can limit solubility in water, making it more soluble in organic solvents.
  • Temperature: Increasing temperature often aids in the dissolution of solid compounds, potentially improving solubility under certain conditions.

To summarize, while this compound may demonstrate some degree of solubility in polar solvents due to polar interactions, its overall solubility may be limited by its hydrophobic regions. Therefore, it is reasonable to expect that:

  • The compound is more likely to dissolve in organic solvents such as dichloromethane or ethyl acetate.
  • It mayhave lower solubility in water, requiring careful consideration when formulating solutions for experimental purposes.

Overall, understanding the solubility profile of this compound is crucial for its applications in various chemical processes and formulations.

Interesting facts

Interesting Facts about 4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]pyridine

This compound represents a unique fusion of aromatic and heterocyclic chemistry, showcasing several fascinating characteristics:

Chemical Structure

  • It features a complex structure that combines a pyridine ring with an imidazole ring, exhibiting intriguing physical and chemical properties.
  • The presence of both fluoro and nitro substituents highlights its potential as a target for various chemical reactions and applications in materials science.
  • This compound's architecture makes it an excellent candidate for exploring structure-activity relationships in medicinal chemistry.

Biological Relevance

  • Similar compounds are often investigated for their action in molecular biology, particularly in cancer research due to their potential to inhibit specific enzymes.
  • The imidazole moiety is known to exhibit biological activity, making this compound a subject of interest for pharmaceuticals.

Synthesis and Applications

  • This compound can be synthesized through various organic chemistry techniques, often involving multi-step processes that highlight the intricacies of pharmaceutical development.
  • Its potential applications could range from biological assays to the development of advanced materials, underscoring the interdisciplinary nature of chemistry.

In summary, 4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]pyridine serves as an intriguing example of the interplay between chemical structures and their potential applications in research and industry.

Synonyms
152121-53-4
PD 169316
PD-169316
PD169316
4-(4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl)pyridine
4-(4-Fluorophenyl)-2-(4-nitrophenyl)-5-(4-pyridyl)-1H-imidazole
4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]pyridine
PD168316
GX3Y2V80CV
2-(4-Nitrophenyl)-4-(4-fluorophenyl)-5-(4-pyridinyl)-1H-imidazole
J1.342.800J
MFCD12405019
Pyridine, 4-(4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl)-
CHEMBL17331
DTXSID8042684
Pyridine, 4-(5-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-4-yl)-
Pyridine, 4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]-
4-(5-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-4-yl)pyridine
UNII-GX3Y2V80CV
C20H13FN4O2
BGIYKDUASORTBB-UHFFFAOYSA-N
CBiol_002019
SCHEMBL154958
GTPL6016
SCHEMBL9899161
DTXCID6022684
CHEBI:93358
EX-A219
BCPP000122
Bio1_000305
Bio1_000794
Bio1_001283
HMS3229M10
HMS3261A04
HMS3649N16
BCP02234
Tox21_500401
BDBM50230001
HSCI1_000116
s5183
AKOS015994573
AKOS016340706
AKOS024464733
BCP9001064
CCG-206874
CCG-221705
CS-1711
ES-0028
FP99820
LP00401
SDCCGSBI-0086779.P002
SDCCGSBI-0086779.P006
NCGC00093828-01
NCGC00093828-02
NCGC00093828-03
NCGC00093828-04
NCGC00093828-05
NCGC00093828-06
NCGC00093828-14
NCGC00261086-01
AC-31396
HY-10578
SY235161
PD169316?
EU-0100401
P2532
PD 169,316
PD 169316, >=98% (HPLC), solid
SR-01000838075
SR-01000838075-3
BRD-K77133231-001-01-1
Q27088275
PD 169316 - CAS 152121-53-4
4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]-pyridine
4-[5-(4-Fluoro-phenyl)-2-(4-nitro-phenyl)-3H-imidazol-4-yl]-pyridine
4-[5-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-4-yl]-pyridine
4-[5-(4-FLUOROPHENYL)-2-(4-NITROPHENYL)-3H-IMIDAZOL-4-YL]PYRIDINE
633-972-5