N-Acetyl-L-aspartic acid

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Identification

Molecular formula
C8H11NO6
CAS Number
997-55-7
IUPAC Name
2-(3-carboxypropanoylamino)pentanedioic acid
Molecular Weight
189.17g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3350g/cm3
Synonyms
SCHEMBL6270974
Interesting facts

Exploring 2-(3-Carboxypropanoylamino)pentanedioic Acid

2-(3-Carboxypropanoylamino)pentanedioic acid is a fascinating compound in the realm of organic chemistry and biochemistry. Here are some compelling facts that showcase its significance:

  • Biological Relevance: This compound plays a crucial role in various metabolic pathways, primarily in amino acid metabolism and synthesis. Its unique structure potentially contributes to the functionality and regulation of enzymes involved in these pathways.
  • Structural Features: The presence of both carboxyl and amino groups in its structure allows it to participate in a range of biochemical reactions, enabling it to function as an intermediate in biosynthetic processes.
  • Potential Applications: Researchers are investigating the use of 2-(3-carboxypropanoylamino)pentanedioic acid in drug designs, particularly in developing therapies for metabolic disorders and diseases related to amino acid imbalances.
  • Synthesis Challenges: The synthesis of this compound can present challenges regarding selectivity and yield due to its complex structure. Understanding its synthesis opens doors to explore new methods in organic chemistry.
  • Research Interest: This compound has attracted attention for further research in fields such as pharmacology and nutrition. Its diverse functional groups make it a perfect candidate for studying molecular interactions.

As you dive deeper into the world of 2-(3-carboxypropanoylamino)pentanedioic acid, you'll discover how remarkable compounds like this can lead to breakthroughs in science and medicine.

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