3-Nitrobiphenyl
- Molecular formula
- C12H9NO2
- CAS Number
- 2113-58-8
- IUPAC Name
- 1-nitro-3-phenyl-benzene
- Molecular Weight
- 199.21g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2040g/cm3
- Synonyms
- 3-Nitrobiphenyl
Identification
Interesting Facts about 1-Nitro-3-phenyl-benzene
1-Nitro-3-phenyl-benzene, often referred to by its IUPAC name, is a fascinating compound in the realm of organic chemistry. As a member of the nitroaromatic family, this compound exhibits unique properties and applications due to the presence of both nitro and phenyl functional groups.
Key Characteristics
- Electrophilic Reactivity: The nitro group (-NO2) attached to the benzene ring significantly enhances its electrophilic character, making it a prime candidate for further chemical reactions.
- Industrial Importance: Compounds like 1-nitro-3-phenyl-benzene serve as intermediates in the synthesis of dyes, pharmaceuticals, and agrochemicals. Their role in chemical manufacturing cannot be overstated.
- Environmental Consideration: As with many nitro compounds, there are environmental and health concerns associated with their use and degradation. Studying these aspects is crucial for ensuring safety in applications.
Chemical Behavior
When exploring the chemical behavior of 1-nitro-3-phenyl-benzene, it is essential to note:
- Its ability to undergo nucleophilic substitution reactions.
- How the position of the nitro group influences the reactivity of the compound.
- The potential for reduced derivatives to form, which can yield further interesting compounds.
Research Significance
This compound serves as a model for understanding:
- Electrophilic aromatic substitution reactions.
- Intermolecular interactions in complex organic systems.
- Insights into the mechanisms of nitro group substitutions.
In summary, 1-nitro-3-phenyl-benzene is not just a simple organic compound; it is a gateway to deeper insights in organic chemistry, providing both challenges and opportunities for research and industrial applications. Its continued study can lead to advancements in synthetic methodologies and chemical safety practices.