nicotinaldehyde oxime
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- Molecular formula
- C6H6N2O
- CAS Number
- 1003-82-5
- IUPAC Name
- pyridine-3-carbaldehyde oxime
- Molecular Weight
- 122.13g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1113g/cm3
- Synonyms
- 3-pyridine aldoxime
Identification
Interesting facts
Interesting Facts about Pyridine-3-carbaldehyde Oxime
Pyridine-3-carbaldehyde oxime is a fascinating compound with a distinct chemical structure and a variety of applications in the field of chemistry. Here are some notable aspects:
- Structure and Isomerism: The compound features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. This unique structure allows for several isomeric forms, which can lead to different chemical behaviors.
- Reactivity: As an oxime, this compound can engage in a variety of reactions, including condensation, which is important in syntheses involving carbon-nitrogen bond formation. This makes it a valuable building block for chemists.
- Applications: Pyridine-3-carbaldehyde oxime plays a significant role in the synthesis of various pharmaceuticals and agrochemicals. It is particularly noted for its utility in developing compounds with potential biological activities.
- Biological Significance: Compounds derived from pyridine bases are often found to exhibit interesting biological properties, including antimicrobial and anti-inflammatory activities, making the study of pyridine derivatives crucial in medicinal chemistry.
- Historical Importance: Pyridine itself was first obtained from coal tar in the 19th century, which paved the way for further research into its derivatives and their reactions, laying the groundwork for modern organic synthesis techniques.
In summary, pyridine-3-carbaldehyde oxime offers intriguing avenues for exploration in both synthetic chemistry and medicinal applications. As chemists continue to investigate its properties and potential uses, it remains an exciting compound in the realm of chemical research.