Dinoseb
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- Molecular formula
- C10H12N2O5
- CAS Number
- 88-85-7
- IUPAC Name
- 2-(1-methylbutyl)-4,6-dinitro-phenol
- Molecular Weight
- 240.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5280g/cm3
- Synonyms
- Dinosam
Identification
Interesting facts
Interesting Facts about 2-(1-methylbutyl)-4,6-dinitro-phenol
2-(1-methylbutyl)-4,6-dinitro-phenol, commonly known as a chemical intermediate, has several notable features that make it an interesting subject of study in the field of chemistry. Below are some engaging facts about this compound:
- Versatile Applications: This compound is primarily utilized in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows it to serve as a building block in the development of new chemical entities.
- Structural Significance: The presence of the dinitro groups on the aromatic ring plays a crucial role in its reactivity. These groups are known for enhancing electrophilic substitution reactions, making the compound a valuable intermediate in organic synthesis.
- Environmental Considerations: As with many nitro compounds, 2-(1-methylbutyl)-4,6-dinitro-phenol raises environmental concerns. Its potential toxicity to aquatic life emphasizes the importance of responsible handling and disposal practices in the laboratory.
- Research Interest: The compound has garnered attention in research for its biological activities, including potential antifungal and antibacterial properties. Scientists continue to explore these characteristics for possible therapeutic applications.
- Structure-Activity Relationship (SAR): Understanding how variations in its structure can impact biological activity is a key area of study. This exploration helps chemists in the design and optimization of more effective compounds.
In summary, 2-(1-methylbutyl)-4,6-dinitro-phenol not only serves a purpose in industrial applications but also presents a fascinating subject for both academic and practical chemistry. The ongoing exploration of its properties and applications reflects the ever-evolving nature of chemical science.