N-Acetylaspartic acid

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Identification

Molecular formula
C6H9NO5
CAS Number
997-55-7
IUPAC Name
2-amino-4-(3-carboxypropanoyloxy)butanoic acid
Molecular Weight
175.15g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1829g/cm3
Synonyms
Homoserine, O-succinyl-
Interesting facts

Interesting Facts about 2-amino-4-(3-carboxypropanoyloxy)butanoic acid

2-amino-4-(3-carboxypropanoyloxy)butanoic acid, commonly recognized for its role in various biological systems, is a fascinating compound worth exploring. Here are some compelling aspects:

  • Biological Significance: This compound plays a critical role as a building block for biosynthesis, closely related to amino acids that are vital for protein structure and function.
  • Functionality: It contains both amino and carboxylic acid functional groups, allowing it to participate in a range of chemical reactions. This dual functionality makes it a versatile molecule in biochemical processes.
  • Metabolic Pathways: Being involved in metabolic pathways, this compound contributes to essential biochemical reactions, which are fundamental for maintaining homeostasis within living organisms.
  • Research Applications: In scientific research, compounds like 2-amino-4-(3-carboxypropanoyloxy)butanoic acid are studied for their potential applications in pharmaceuticals and therapeutic developments. Their biochemical properties can lead to novel treatments for various diseases.
  • Synthetic Utility: Chemists often explore the synthesis of this molecule because of its complex structure, which provides valuable insights into organic synthesis techniques and methodologies.

In conclusion, the diversity and significance of 2-amino-4-(3-carboxypropanoyloxy)butanoic acid make it an intriguing subject of study in the fields of chemistry and biology. As it bridges the gap between biological functions and synthetic applications, it stands out as a compound rich in potential discoveries.

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