Interesting facts
Interesting Facts about 2-Aminopent-4-enoic Acid
2-Aminopent-4-enoic acid, often referred to in scientific discussions, is a fascinating compound with a variety of unique traits that make it valuable in several fields:
- Biochemical Relevance: This compound is structurally related to amino acids and plays a pivotal role in the biosynthesis of various biologically significant molecules. Its structure includes both an amine group and a carboxylic acid group, which are essential for a multitude of metabolic processes.
- Potential Dietary Impact: As a derivative of an amino acid, 2-aminopent-4-enoic acid has implications in nutrition and health, raising interest among researchers exploring the connection between amino acids and human physiology.
- Applications in Synthesis: This compound serves as a crucial intermediate in organic synthesis, particularly in the production of more complex molecules for pharmaceuticals. Its inherent reactivity allows it to participate in various chemical transformations.
- Research and Development: Many studies are currently focused on this compound due to its potential applications in drug design and development, offering promising avenues in medicinal chemistry.
- Environmental Considerations: The relevance of 2-aminopent-4-enoic acid may extend to environmental chemistry, where it could play a role in understanding natural processes and the behavior of organic compounds in ecosystems.
As scientists and students delve deeper into the properties and applications of 2-aminopent-4-enoic acid, its significance in both biological systems and synthetic chemistry continues to be a topic of great interest. Its multifunctional characteristics not only underscore its versatility but also reflect the intricate connections between chemical structure and biological function.
Synonyms
7685-44-1
2-Amino-4-pentenoic acid
ALLYLGLYCINE
1069-48-3
dl-c-Allylglycine
4-Pentenoic acid, 2-amino-
dl-2-Amino-1-pentenoic acid
EINECS 231-689-8
NSC 20898
AI3-52415
wnnnwfkqckfsdk-uhfffaoysa-n
DL-Allylglycine
2-aminopent-4-enoic acid
Dl-2-Amino-4-Pentenoic Acid
DL-2-Allylglycine
MFCD00063103
H-Allyl-DL-glycine
4-Pentenoic acid, 2-amino-, (+/-)-
(R)-2-Allylglycine
C5H9NO2
DL-2-Aminopent-4-enoic acid
2-allylglycine
allyl-C-glycine
MFCD00063104
alpha-allylglycine
H-Allyl-D-glycine
H-Allyl-L-glycine
alpha-Allyl-Gly-OH
2-Allyl-DL-glycine
SCHEMBL44428
CHEMBL4096969
CHEBI:231241
CHEBI:231976
DTXSID701313217
BCP04800
NSC20898
NSC70870
NSC-20898
NSC-70870
AKOS000197494
AKOS016842838
AB88392
AB89048
HY-W023493
AS-56631
BP-12843
SY008709
SY052428
SY064478
4-Pentenoic acid, 2-amino-, (.+/-.)-
A2663
CS-0060001
NS00044687
EN300-49121
O10661
Q4733443
F8881-3848
Z317024964
Solubility of 2-aminopent-4-enoic acid
2-aminopent-4-enoic acid, also known as 5-amino-4-pentenoic acid, exhibits interesting solubility characteristics primarily due to its functional groups. Here are some key points regarding its solubility:
Based on these factors, it can be concluded that 2-aminopent-4-enoic acid is sufficiently soluble in water, contributing to its potential applications in biological systems and as an intermediate in synthetic processes. However, solubility may vary with temperature and concentration, indicating the necessity of empirical testing for precise determinations.