2-(3,4-Dichlorophenyl)-1,3-benzoxazole
- Molecular formula
- C13H7Cl2NO
- CAS Number
- 16110-09-1
- IUPAC Name
- 2-(3,4-dichlorophenyl)-1,3-benzoxazole
- Molecular Weight
- 268.10g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4730g/cm3
- Synonyms
- 2-(3, 4-Dichlorophenyl)benzoxazole
Identification
Exploring 2-(3,4-Dichlorophenyl)-1,3-benzoxazole
2-(3,4-Dichlorophenyl)-1,3-benzoxazole is a fascinating organic compound that falls within the realm of heterocyclic chemistry. Its structure is characterized by a benzoxazole ring system, which is notable for its unique properties and applications.
Key Features:
- Heterocyclic Structure: The compound contains a fused benzene and oxazole ring, imparting distinctive *electronic* and *optical* characteristics.
- Chlorination: The presence of chlorine atoms enhances its reactivity and can influence its interaction with biological systems, making it of interest in medicinal chemistry.
- Fluorescence: Compounds like 2-(3,4-Dichlorophenyl)-1,3-benzoxazole are often investigated for their *fluorescent properties*, which can be harnessed in various applications, including sensors and fluorescent probes.
- Biological Activity: Research indicates that benzoxazole derivatives possess a range of pharmacological activities, including *anti-inflammatory*, *antimicrobial*, and *anticancer* effects, suggesting potential therapeutic applications.
As with many organic compounds, the synthesis of 2-(3,4-Dichlorophenyl)-1,3-benzoxazole typically involves coupling reactions that can be optimized for efficiency and yield. The exploration of its properties and potential uses can lead to significant advancements in both *industry* and *research*. As stated by chemists, “The beauty of chemistry lies not only in its complexity but also in its endless possibilities.”
In summary, 2-(3,4-Dichlorophenyl)-1,3-benzoxazole exemplifies the interplay between structure and function within organic compounds, providing a platform for innovation in various fields of science.