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N-(2-Carboxybenzoyl)glutamate

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Identification
Molecular formula
C13H12NO72-
CAS number
25990-18-9
IUPAC name
2-[(2-carboxylatobenzoyl)amino]pentanedioate
State
State

At room temperature, N-(2-Carboxybenzoyl)glutamate typically exists in a solid state. It's a crystalline compound due to the interactions between its multiple carboxylate and amide functional groups.

Melting point (Celsius)
265.00
Melting point (Kelvin)
538.15
Boiling point (Celsius)
642.00
Boiling point (Kelvin)
915.15
General information
Molecular weight
297.26g/mol
Molar mass
297.2560g/mol
Density
1.5000g/cm3
Appearence

The compound generally appears as a white to off-white crystalline powder. It is often solid in form due to its molecular structure and the presence of carboxylate groups.

Comment on solubility

Solubility of C13H12NO72-

The solubility of 2-[(2-carboxylatobenzoyl)amino]pentanedioate (C13H12NO72-) is influenced by several factors that characterize its chemical nature and interactions in solution.

Key Factors Affecting Solubility:

  • Polarity: The presence of carboxylate groups typically increases polarity, facilitating solubility in polar solvents like water.
  • Ionization: As a dianion, C13H12NO72- may show higher solubility in basic conditions, where it remains ionized.
  • Hydrogen Bonding: The carboxylic acids present can engage in hydrogen bonding with water molecules, enhancing solubility.

In aqueous solutions, the solubility characteristics can be summarized as follows:

  1. Higher solubility at elevated pH levels due to increased ionization.
  2. Limited solubility in non-polar solvents because of its polar functional groups.

These properties collectively suggest that C13H12NO72- is likely to be soluble in polar solvents, making it applicable for various biochemical and synthetic processes. Understanding these solubility dynamics is essential for effectively utilizing this compound in chemical applications.

Interesting facts

Interesting Facts about 2-[(2-carboxylatobenzoyl)amino]pentanedioate

2-[(2-carboxylatobenzoyl)amino]pentanedioate, often referred to in the scientific community as a specialized derivative of amino acids, is a fascinating compound that bridges the worlds of organic chemistry and biochemical applications. Below are some captivating insights about this compound:

  • Versatile Applications: This compound plays a significant role in the synthesis of pharmaceuticals and agrochemicals. Its unique structure allows for various modifications that enhance biological activity.
  • Biochemical Relevance: The presence of a carboxyl group makes it an important player in metabolic pathways. It can interact effectively with biological systems due to its capability to form hydrogen bonds.
  • Research Frontier: Scientists are continuously exploring its potential in medicinal chemistry, particularly in drug development targeting enzymes and receptors due to its specific molecular characteristics.
  • Structure-Activity Relationship: The compound's structure aids in understanding the relationship between its chemical properties and biological activities, making it a topic of interest in pharmacology.
  • Theoretical Insights: Computational chemistry models often utilize this compound to predict behavior based on its complex molecular structure, which can lead to innovative discoveries.

Moreover, the intricate balance of acidic and basic groups within this compound contributes to its ionization behavior, further emphasizing its utility in biochemical interactions. As noted by one researcher, “Understanding the nuances of compounds like 2-[(2-carboxylatobenzoyl)amino]pentanedioate can unlock new therapeutic pathways.”

In summary, this compound not only exemplifies the beauty of chemical diversity but also opens doors to advancements in scientific research, particularly in the fields of drug discovery and metabolic engineering. The ongoing studies surrounding its properties and potential applications continue to fascinate chemists and biologists alike.

Synonyms
CCG-205098