Interesting Facts About 2-[(2-carboxybenzoyl)amino]pentanedioic Acid
2-[(2-carboxybenzoyl)amino]pentanedioic acid, often referred to as a derivative of amino acids, is a fascinating compound that showcases the intricate relationship between structure and function in organic chemistry. This compound is notable for several reasons:
- Biological Significance: As a derivative of amino acids, it plays potential roles in biological systems and can serve as a metabolic intermediate in various biochemical pathways.
- Pharmaceutical Applications: Research suggests that compounds with similar structures may have therapeutic benefits, potentially acting as anti-inflammatory or analgesic agents.
- Synthetic Versatility: This compound can be synthesized through various organic reactions, making it a key player in the field of organic synthesis and drug design.
- Structural Complexity: The presence of carboxylic acid groups gives this compound unique properties, offering opportunities for complex molecular interactions.
Additionally, compounds like 2-[(2-carboxybenzoyl)amino]pentanedioic acid are often utilized in research studies to better understand protein interactions and the behavior of biomolecules in different environments. This highlights the importance of studying small molecules in the vast context of molecular biochemistry.
In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have lots of ideas.” This resonates well with the exploration of compounds such as this, as they continue to inspire chemists and researchers in their quest for novel applications and deeper understanding.
Solubility of 2-[(2-carboxybenzoyl)amino]pentanedioic acid (C13H11NO6)
The solubility of 2-[(2-carboxybenzoyl)amino]pentanedioic acid is an intriguing topic due to its complex structure and functional groups. This compound, possessing both carboxylic acid and amine functional groups, exhibits *unique solubility characteristics*. Here are some key points to consider:
As a point of interest, the solubility can be influenced significantly by pH levels. At higher pH conditions, the carboxylic groups may deprotonate, increasing the overall solubility in aqueous solutions.
In conclusion, the solubility behavior of 2-[(2-carboxybenzoyl)amino]pentanedioic acid is a testament to the intricate balance of molecular interactions that dictate a compound's behavior in various solvents.