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Methyl 4-chlorophenylalanine

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Identification
Molecular formula
C10H12ClNO2
CAS number
6635-50-7
IUPAC name
methyl 2-amino-3-(4-chlorophenyl)propanoate
State
State

At room temperature, Methyl 4-chlorophenylalanine is a solid.

Melting point (Celsius)
84.00
Melting point (Kelvin)
357.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
213.67g/mol
Molar mass
213.6700g/mol
Density
1.2710g/cm3
Appearence

The compound appears as a white crystalline solid, often in fine powder form. It may have a characteristic odor typical of amino acid derivatives.

Comment on solubility

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:

  • Polarity: Methyl 2-amino-3-(4-chlorophenyl)propanoate contains both polar and nonpolar regions in its structure. The presence of the amino group (-NH2) typically increases polarity, potentially enhancing its solubility in polar solvents such as water.
  • Solvent Interaction: While the compound may dissolve in water, it may also show different solubility levels in organic solvents. For instance, solvents like ethanol could solvate the molecule more effectively due to similar polar characteristics.
  • Influence of Substituents: The 4-chlorophenyl group introduces a hydrophobic character, which can hinder solubility in highly polar solvents but enhance solubility in less polar, organic solvents. This dual nature can lead to varying solubility outcomes depending on the solvent used.
  • Temperature Dependency: It is essential to consider that temperature can significantly affect solubility. Generally, higher temperatures can lead to increased solubility in most solid solutes.

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.

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