Interesting facts
Interesting Facts about Methyl 2-Amino-3-(4-Chlorophenyl)propanoate
Methyl 2-amino-3-(4-chlorophenyl)propanoate, commonly referred to in research as a derivative of amino acid compounds, showcases a fascinating intersection between organic chemistry and medicinal applications. Here are some compelling insights:
- Biological Relevance: This compound is often studied for its potential therapeutic applications, particularly in the areas of neurology and psychiatry. It can serve as a starting point for creating pharmaceuticals aimed at treating various central nervous system disorders.
- Synthetic Versatility: The structure of this compound allows for diverse synthetic routes, making it an attractive target for chemists looking to modify its properties for enhanced activity. This flexibility in synthesis contributes to its popularity in the field of medicinal chemistry.
- Substituent Effects: The presence of the 4-chlorophenyl group introduces interesting electronic and steric effects. Understanding how such substituents influence the compound's reactivity can open doors to novel applications.
- Enantiomeric Form: This compound can exist in enantiomeric forms, prompting studies into the chiral nature of pharmaceuticals. The differences in activity between enantiomers emphasize the importance of chirality in drug development.
- Research Potential: It serves as a key substance in research focusing on amine chemistry, which is pivotal in organic synthesis and materials science. The various properties that can be explored reflect the compound's importance in the chemical landscape.
In summary, methyl 2-amino-3-(4-chlorophenyl)propanoate is more than just a molecule; it represents a bridge between basic chemical research and applied pharmaceutical innovation. As stated by many researchers, “Understanding the nuances of such compounds can lead to breakthrough therapies and enhanced quality of life.”
Synonyms
23434-96-0
Phenylalanine, 4-chloro-, methyl ester
p-Chlorophenylalanine methyl ester
4-Chlorophenylalanine methyl ester
ALANINE, 3-(p-CHLOROPHENYL)-, METHYL ESTER
ZA5R0QT27X
H69/17
para-chlorophenylalanine methyl ester
Methyl 2-amino-3-(4-chlorophenyl)propanoate
4-chloro-dl-phenylalanine methyl ester
CCRIS 8841
Methyl 4-chloro-3-phenylalaninate
EINECS 245-661-8
UNII-ZA5R0QT27X
BRN 3032592
methyl2-amino-3-(4-chlorophenyl)propanoate
Lopac0_000311
SCHEMBL2734777
CHEMBL1354719
DTXSID00946090
dl-4-chlorophenylalanine methyl ester
dl-p-chlorophenylalanine methyl ester
AKOS005174355
CCG-204406
SDCCGSBI-0050299.P002
NCGC00015231-02
NCGC00015231-03
NCGC00015231-06
NCGC00162123-01
methyl 4-chlorophenylalaninate hydrochloride
CS-0449871
NS00051283
E73731
Methyl 2-amino-3-(4-chlorophenyl)propanoate #
EN300-1069057
AE-641/30398005
Q27295205
2-Amino-3-(4-chlorophenyl)-propionic acid methyl ester
Solubility of Methyl 2-amino-3-(4-chlorophenyl)propanoate
The solubility of methyl 2-amino-3-(4-chlorophenyl)propanoate is an important factor in understanding its behavior in various environments. This compound, commonly known as a derivative of amino acids, exhibits unique solubility characteristics influenced by its molecular structure.
Key Points on Solubility:
In conclusion, while methyl 2-amino-3-(4-chlorophenyl)propanoate may be soluble in both polar and nonpolar solvents, its solubility behavior should be closely examined within the context of specific applications and conditions. Understanding these nuances will optimize usage and manipulation of this compound in chemical processes.