Interesting facts
Interesting Facts about 1-(2-Nitrophenyl)butane-1,3-dione
1-(2-Nitrophenyl)butane-1,3-dione is a fascinating compound that falls within the class of diketones, known for their unique chemical structures and reactivity. Here are some intriguing insights about this compound:
- Structural Characteristics: The presence of a nitro group at the 2-position of the phenyl ring plays a crucial role in its reactivity, significantly influencing its electronic properties. This substitution can enhance the compound's ability to undergo electrophilic reactions.
- Potential Applications: Diketones like 1-(2-nitrophenyl)butane-1,3-dione are valued in various fields. They are often utilized as:
- Intermediates in the synthesis of pharmaceuticals.
- Key building blocks for the development of organic materials.
- Active components in agrochemicals and dyes.
- Reactivity: The compound is known to participate in various organic reactions, including:
- Condensation reactions, where it may react with different nucleophiles.
- Formation of complex compounds through coordination with transition metals, making it an interesting candidate for coordination chemistry.
- Research Significance: Compounds like this are often studied for their biochemical properties, revealing potential roles in medicinal chemistry. Research may explore their capabilities as:
- Enzyme inhibitors, targeting specific biological pathways.
- Antioxidants, due to their ability to stabilize free radicals.
- Environmental Impact: Given its potential use in agrochemicals, understanding the environmental persistence and degradation pathways of 1-(2-nitrophenyl)butane-1,3-dione becomes crucial. Scientists investigate how such compounds affect ecosystems and human health.
This compound is more than just a chemical formula; its distinct properties and applications make it a subject of ongoing study and interest within the fields of chemistry and material science. As research advances, we continue to uncover the profound implications of diketones in various domains.
Synonyms
1-(2-nitrophenyl)butane-1,3-dione
5463-78-5
1,3-BUTANEDIONE, 1-(o-NITROPHENYL)-
1,3-Butanedione, 1-(2-nitrophenyl)-
1-(o-Nitrophenyl)-1,3-butanedione
1-(2-Nitrophenyl)-1,3-butanedione
C7D6JJ4Y6C
NSC-21484
NSC 21484
BRN 1877907
NSC21484
o-Nitrobenzoylaceton
UNII-C7D6JJ4Y6C
WLN: WNR B1VV1
1, 1-(o-nitrophenyl)-
1, 1-(2-nitrophenyl)-
SCHEMBL8488879
DTXSID00969906
AKOS009269001
1,3-Butanedione,1-(2-nitrophenyl)-
EN300-1126234
Solubility of 1-(2-nitrophenyl)butane-1,3-dione
1-(2-nitrophenyl)butane-1,3-dione is a compound that exhibits interesting solubility characteristics due to its unique structure. Understanding its solubility is vital for applications in various chemical processes.
General Solubility Characteristics
The solubility of 1-(2-nitrophenyl)butane-1,3-dione can be influenced by several factors:
Solvent Compatibility
1-(2-nitrophenyl)butane-1,3-dione is generally:
In conclusion, while 1-(2-nitrophenyl)butane-1,3-dione exhibits a degree of solubility in polar organic solvents, its overall solubility profile reflects its complex interplay of hydrophilic and hydrophobic factors. As the saying goes, “Like dissolves like,” and this compound’s solubility really emphasizes that principle!