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Methyl Tyrosinate

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Identification
Molecular formula
C11H15NO3
CAS number
6673-14-1
IUPAC name
methyl 2-amino-3-(4-hydroxyphenyl)-2-methyl-propanoate
State
State

At room temperature, methyl tyrosinate is generally in a solid state. It is stable under normal conditions of temperature and pressure.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
332.70
Boiling point (Kelvin)
605.85
General information
Molecular weight
209.24g/mol
Molar mass
209.2330g/mol
Density
1.2260g/cm3
Appearence

The compound typically appears as a white to off-white powder. Its texture is crystalline, and it is often used in research chemistry. It may have a slight aromatic odor due to the phenyl component in its structure.

Comment on solubility

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:

  • Polarity: The presence of the amino group (-NH2) and the hydroxy group (-OH) contributes to the overall polarity of the molecule, enhancing its solubility in polar solvents, particularly water.
  • Hydrogen Bonding: Due to the hydroxy and amino functional groups, the compound is capable of forming hydrogen bonds. This greatly facilitates its dissolution in solvents capable of engaging in similar interactions.
  • Hydrophobic Interactions: The hydrocarbon portions of the molecule, including the methyl groups, can limit solubility in non-polar solvents, leading to a preferential solubility in polar environments.

As a result, one may find that:

  • Methyl 2-amino-3-(4-hydroxyphenyl)-2-methyl-propanoate is more soluble in aqueous solutions.
  • It shows limited solubility in non-polar organic solvents, which is typical for such compounds that balance polar and non-polar characteristics.

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.

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