(2,4-Dinitrophenyl)methanol
- Molecular formula
- C7H6N2O4
- CAS Number
- 6342-45-4
- IUPAC Name
- (2,4-dinitrophenyl)methanol
- Molecular Weight
- 198.14g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5280g/cm3
- Synonyms
- 2, 4-Dinitrobenzyl alcohol
Identification
Interesting Facts about (2,4-Dinitrophenyl)methanol
(2,4-Dinitrophenyl)methanol is a fascinating compound that has garnered the attention of chemists for its unique structure and applications. This compound illustrates the beautiful intertwining of organic chemistry and analytical techniques.
Key Characteristics
- Versatile Reagent: (2,4-Dinitrophenyl)methanol is widely used as a reagent in organic synthesis, often utilized in the detection and analysis of various functional groups.
- Colorimetric Indicator: Remarkably, it can act as a colorimetric indicator, enabling researchers to visually assess chemical reactions based on changes in color.
- Environmental Impact: As a dinitro compound, it raises discussions regarding its environmental impact, particularly regarding its potential toxicity and the need for careful handling.
- Historical Significance: The dinitrophenyl moiety itself has historical significance, particularly in the context of early experiments in chemical warfare during World War I.
Applications in Research
This compound has been utilized in various fields of research, including:
- Analytical Chemistry: It is instrumental in analytical chemistry for quantifying alcohols, as the reaction yields a colored product that allows for easy measurement.
- Pharmaceutical Development: In medicinal chemistry, (2,4-Dinitrophenyl)methanol can be a starting material for synthesizing various pharmaceuticals and other biologically active compounds.
In summary, this compound stands as a testament to the intricate relationship between molecular structure and functionality in organic chemistry. As one explores the complexities of (2,4-Dinitrophenyl)methanol, it becomes clear that this compound is not just a mere chemical entity but a resourceful tool in modern chemical research.