4-(2-Aminophenyl)-2,4-dioxobutanoic acid, also known as APDB, is a compound that has garnered interest in the fields of pharmaceuticals and medicinal chemistry due to its potential as a building block for novel drug development. Specifically, APDB has shown promise in inhibiting certain enzymes and receptors involved in diseases such as cancer and neurodegenerative disorders. While the direct impact of APDB on everyday life may not be readily apparent, its potential to lead to the development of new treatments for debilitating conditions highlights its relevance in improving overall health and well-being.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
4-(2-Aminophenyl)-2,4-dioxobutanoic acid, commonly known as ABDA, has various commercial and industrial applications. It is often used as a precursor in the synthesis of pharmaceuticals, dyes, and perfumes due to its versatile chemical structure. Additionally, ABDA is utilized in the production of specialty chemicals and polymers for a wide range of industrial applications.
In the realm of drug and medication applications, 4-(2-Aminophenyl)-2,4-dioxobutanoic acid plays a crucial role in the development of certain medications. ABDA is utilized in the synthesis of pharmaceutical compounds that have potential therapeutic effects for various medical conditions. The compound’s unique chemical properties make it valuable in the pharmaceutical industry for creating novel drug formulations.
Moreover, 4-(2-Aminophenyl)-2,4-dioxobutanoic acid is employed in the production of certain medications for treating specific health conditions. ABDA is utilized as a key building block in the synthesis of pharmaceuticals with anti-inflammatory, analgesic, or antibacterial properties. Its chemical composition and reactivity make it an essential component in the pharmaceutical manufacturing process.
⚗️ Chemical & Physical Properties
4-(2-Aminophenyl)-2,4-dioxobutanoic acid is a white crystalline solid with no distinct odor. It typically appears as fine powder particles under normal conditions.
This compound has a molar mass of approximately 217.21 g/mol and a density of around 1.41 g/cm3. In comparison to common household items, the molar mass is similar to that of sucrose (table sugar), while the density is comparable to that of baking soda.
The melting point of 4-(2-Aminophenyl)-2,4-dioxobutanoic acid is around 220-222°C, and its boiling point is approximately 624°C. These values are higher than those of most common household items, such as water and cooking oils.
4-(2-Aminophenyl)-2,4-dioxobutanoic acid is sparingly soluble in water and has a relatively high viscosity. Its solubility in water is lower compared to substances like salt and sugar, and its viscosity is higher than that of water and alcohol.
🏭 Production & Procurement
4-(2-Aminophenyl)-2,4-dioxobutanoic acid is typically produced through a multistep synthesis process in the laboratory. The starting materials for this synthesis often include readily available compounds such as 2-aminobenzoic acid and ethyl acetoacetate. These starting materials undergo various chemical reactions, including condensation and cyclization, to ultimately yield 4-(2-Aminophenyl)-2,4-dioxobutanoic acid as the final product.
To procure 4-(2-Aminophenyl)-2,4-dioxobutanoic acid commercially, interested parties may turn to specialized chemical suppliers or manufacturers. This compound is not typically found in common household products or natural sources. Once procured, 4-(2-Aminophenyl)-2,4-dioxobutanoic acid can be transported in accordance with standard regulations governing the transportation of chemical substances. Due to its chemical nature, proper safety precautions must be observed during handling and transportation to prevent any accidents or mishaps that may pose a risk to individuals or the environment.
In the realm of research and pharmaceutical development, 4-(2-Aminophenyl)-2,4-dioxobutanoic acid may be utilized as a key building block in the synthesis of more complex molecules or as a precursor for drug discovery projects. The procurement of this compound may therefore play a crucial role in advancing scientific knowledge and understanding in various fields. Researchers and scientists involved in such endeavors must exercise caution and rigorous adherence to safety protocols when working with 4-(2-Aminophenyl)-2,4-dioxobutanoic acid to ensure the integrity of their work and the safety of those involved in its handling and usage.
⚠️ Safety Considerations
Safety considerations for 4-(2-Aminophenyl)-2,4-dioxobutanoic acid include the need for appropriate personal protective equipment, such as gloves and goggles, to prevent skin and eye contact. This compound should be handled in a well-ventilated area to avoid inhalation of harmful vapors. Additionally, care should be taken when storing this compound to prevent accidental spills or leaks.
The pharmacology of 4-(2-Aminophenyl)-2,4-dioxobutanoic acid involves its role as a potential drug candidate for the treatment of various diseases. Studies have shown that this compound exhibits promising anti-inflammatory and antioxidant properties, which may be beneficial in combating conditions such as arthritis and cardiovascular disease. Further research is needed to fully understand the mechanism of action and potential therapeutic applications of this compound.
Hazard statements for 4-(2-Aminophenyl)-2,4-dioxobutanoic acid include its classification as a skin and eye irritant. Prolonged or repeated exposure to this compound may cause irritation, redness, or chemical burns. In case of contact, immediate rinsing with plenty of water is recommended, and medical attention should be sought if symptoms persist.
Precautionary statements for 4-(2-Aminophenyl)-2,4-dioxobutanoic acid include the importance of wearing appropriate protective clothing and respiratory equipment when handling this compound. It is advisable to work with this compound in a fume hood or well-ventilated area to minimize exposure to harmful vapors. Proper storage and handling procedures should be followed to prevent accidents and ensure the safety of individuals working with this compound.
🔬 Potential Research Directions
One potential research direction for 4-(2-Aminophenyl)-2,4-dioxobutanoic acid is its application as a potential drug candidate for the treatment of certain medical conditions. Further studies could investigate its pharmacological properties and potential therapeutic effects.
Another area of interest could be the exploration of the chemical reactivity and biological activity of 4-(2-Aminophenyl)-2,4-dioxobutanoic acid. This could involve synthesizing derivatives of the compound to study their effects on different biological systems.
Additionally, research could focus on the potential role of 4-(2-Aminophenyl)-2,4-dioxobutanoic acid in various biochemical pathways and its interactions with other molecules. Understanding its mechanism of action could provide valuable insights for drug development and therapeutic interventions.
Moreover, investigations into the potential toxicity and safety profile of 4-(2-Aminophenyl)-2,4-dioxobutanoic acid could be crucial for its future development as a pharmaceutical agent. Studying its effects on different cell lines and animal models could help assess its potential risks and benefits.
🧪 Related Compounds
One similar compound to 4-(2-Aminophenyl)-2,4-dioxobutanoic acid based upon molecular structure is 4-(3-Aminophenyl)-2,4-dioxobutanoic acid. In this compound, the amino group is located at the third position on the phenyl ring instead of the second position. This slight variation in the location of the amino group may result in differences in the compound’s chemical properties and biological activity.
Another similar compound is 4-(2-Aminophenyl)-3,4-dioxobutanoic acid. In this compound, the carbonyl group is located at the third position on the butanoic acid chain instead of the fourth position. This structural difference may lead to changes in the compound’s reactivity and ability to bind to biological targets.
Additionally, a related compound is 3-(2-Aminophenyl)-2,4-dioxobutanoic acid. In this compound, the phenyl ring is attached to the butanoic acid chain at the third position rather than the fourth position. This alteration in the position of the phenyl group may impact the compound’s solubility, stability, and interaction with other molecules in biological systems.