2,3,6-Trichlorobenzaldehyde
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- Molecular formula
- C7H3Cl3O
- CAS Number
- 1009-02-9
- IUPAC Name
- 2,3,6-trichlorobenzaldehyde
- Molecular Weight
- 209.46g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5064g/cm3
- Synonyms
- 2, 3, 6-TRICHLOROBENZALDEHYDE
Identification
Interesting facts
Interesting Facts about 2,3,6-Trichlorobenzaldehyde
2,3,6-Trichlorobenzaldehyde is a fascinating organic compound that has garnered significant attention in the fields of chemistry and materials science. Here are some intriguing insights into this compound:
- Structural Features: The presence of three chlorine atoms on its benzene ring dramatically influences its reactivity and properties, making it a valuable building block in organic synthesis.
- Pharmaceutical Applications: Due to its unique structure, 2,3,6-trichlorobenzaldehyde is often explored in the development of various pharmaceutical agents. Its reactivity can facilitate the synthesis of complex organic molecules required for drug development.
- Environmental Considerations: Chlorinated compounds, such as this one, are of interest when assessing environmental toxicity. Understanding their behavior in environmental systems is essential for evaluating their safety and potential impacts.
- Research Interest: The compound's ability to act as a precursor in the synthesis of more complex organic molecules has made it a subject of numerous research studies aimed at developing novel chemical methodologies.
- Distinctive Odor: Like many aldehydes, 2,3,6-trichlorobenzaldehyde possesses a characteristic odor which can be utilized in various applications requiring fragrance or flavor profiles.
Overall, 2,3,6-trichlorobenzaldehyde stands out not only for its structural uniqueness but also for its versatility in multiple fields, ranging from synthetic chemistry to environmental science. As one dives deeper into the world of organic compounds, exploring the applications and implications of such chlorinated derivatives becomes essential for a holistic understanding of chemical interactions.