Interesting facts
Interesting Facts about Methyl 2-Amino-3-(4-Hydroxyphenyl)-2-Methyl-Propanoate
Methyl 2-amino-3-(4-hydroxyphenyl)-2-methyl-propanoate, often noted for its intriguing structure and potential applications, belongs to the class of amino acid derivatives. Here are some fascinating insights about this compound:
- Diverse Applications: This compound can be utilized in pharmaceuticals due to its potential medicinal properties. It's often explored for its roles in drug development, especially concerning analgesic and anti-inflammatory agents.
- Structural Significance: The presence of both amino and hydroxyl functional groups suggests that this compound can participate in various chemical reactions, making it a versatile building block in organic synthesis.
- Biological Relevance: Methyl 2-amino-3-(4-hydroxyphenyl)-2-methyl-propanoate has been studied for its interactions with biological systems. Its structure hints at possible activities similar to known neurotransmitters, which can influence mood and cognitive functions.
- Research Potential: As a subject of scientific research, this compound often finds itself in studies aiming to enhance the effectiveness of existing drugs or to design new therapeutic agents based on its unique properties.
- Functionality in Reactions: It can serve as a versatile reagent in the synthesis of more complex molecules due to the ease with which its functional groups can be manipulated.
In the realm of chemistry, compounds like methyl 2-amino-3-(4-hydroxyphenyl)-2-methyl-propanoate remind us of the delicate balance between structure and function. As noted by many chemists, “The features of a compound dictate not just its properties but also the pathways to new discoveries.” Exploring this compound further could lead to significant breakthroughs in medicinal chemistry and beyond.
Synonyms
alpha-Methyltyrosine methyl ester
4502-13-0
racemetirosine methyl ester
N73778YX9N
alpha-Methylparatyrosine methylester
alpha-Methyl-DL-tyrosine methyl ester
DL-Tyrosine, alpha-methyl-, methyl ester
UNII-N73778YX9N
alpha-Methyl-p-tyrosine methyl ester
alpha-Methyl-para-tyrosine methyl ester
Tyrosine, .alpha.-methyl-, methyl ester
Maybridge3_005374
Methyl alpha-methyltyrosinate
Lopac0_000785
SCHEMBL503526
CHEMBL1181010
DTXSID20963325
METHYL ALPHA-METHYLTYROSINE
alpha-Methyltyrosine, methyl ester
Tyrosine, alpha-methyl-, methyl ester
CCG-204870
SDCCGSBI-0050763.P002
IDI1_016761
NCGC00015667-02
NCGC00015667-03
NCGC00015667-04
NCGC00162254-01
METHYL DL-.ALPHA.-METHYLTYROSINATE
PD034335
.ALPHA.-METHYL-DL-P-TYROSINE METHYL ESTER
(+/-)-.ALPHA.-METHYL-P-TYROSINE METHYL ESTER
Q27284649
Solubility of Methyl 2-amino-3-(4-hydroxyphenyl)-2-methyl-propanoate
Methyl 2-amino-3-(4-hydroxyphenyl)-2-methyl-propanoate, with the chemical formula C11H15NO3, exhibits unique solubility characteristics that can be attributed to its molecular structure.
When considering the solubility of this compound, several factors come into play:
As a result, one may find that:
In conclusion, the solubility of this compound is influenced by its ability to form hydrogen bonds and its structural composition. This balance between polar and non-polar regions makes it an important candidate for investigations in various scientific applications.