4,6-Dichloro-2-(trifluoromethyl)-1H-benzimidazole
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- Molecular formula
- C8H3Cl2F3N2
- CAS Number
- 51395-75-6
- IUPAC Name
- 4,6-dichloro-2-(trifluoromethyl)-1H-benzimidazole
- Molecular Weight
- 251.99g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.6391g/cm3
- Synonyms
- 4228-88-0
Identification
Interesting facts
Interesting Facts about 4,6-Dichloro-2-(trifluoromethyl)-1H-benzimidazole
4,6-Dichloro-2-(trifluoromethyl)-1H-benzimidazole is a fascinating compound in the realm of organic chemistry, particularly known for its structural complexity and potential applications. Below are some intriguing aspects of this compound:
- Structural Features: This compound is characterized by the presence of a benzimidazole core, which is a bicyclic structure consisting of a fused benzene and imidazole ring. The presence of both chlorine and a trifluoromethyl group at specific positions highlights the *diversity of functionalization* possible within this class of compounds.
- Biological Activities: Compounds like 4,6-dichloro-2-(trifluoromethyl)-1H-benzimidazole have been studied for their *antimicrobial* and *antiparasitic* properties. Benzimidazoles are known to exhibit significant bioactivity, making them of interest in pharmaceutical research.
- Fluorine's Role: The trifluoromethyl group, a common motif in drug design, can enhance *lipophilicity* and *bioavailability*. The introduction of fluorine atoms can also alter the acidity, reactivity, and overall metabolism of the compound, providing an opportunity for innovative therapeutic strategies.
- Applications in Agriculture: Due to their efficacy, benzimidazole derivatives are utilized in agriculture as fungicides and herbicides, contributing to crop protection and yield enhancement. Such compounds are pivotal in ensuring food security.
- Research Potential: The unique set of functional groups in this compound creates a platform for further modification and exploration. Researchers continue to investigate its potential for developing new materials, catalysts, and therapeutic agents.
In summary, 4,6-dichloro-2-(trifluoromethyl)-1H-benzimidazole exemplifies the importance of structural diversity in medicinal chemistry and agricultural sciences. The ongoing exploration of its properties can lead to the development of innovative solutions in various fields.