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Methyl 3,5-diiodo-L-tyrosinate

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Identification
Molecular formula
C10H11I2NO3
CAS number
13812-68-5
IUPAC name
methyl 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoate
State
State

Solid form at room temperature.

Melting point (Celsius)
228.00
Melting point (Kelvin)
501.15
Boiling point (Celsius)
405.00
Boiling point (Kelvin)
678.15
General information
Molecular weight
483.97g/mol
Molar mass
483.9660g/mol
Density
2.1422g/cm3
Appearence

Off-white or light yellow crystalline powder.

Comment on solubility

Solubility of Methyl 2-Amino-3-(4-Hydroxy-3,5-Diiodo-Phenyl)Propanoate

The solubility of methyl 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoate can be influenced by several factors due to its complex structure. This compound features both hydrophilic and hydrophobic characteristics, which significantly affect its solubility in various solvents. Below are some key points regarding its solubility:

  • Solvent Dependence: It is generally expected to have higher solubility in polar solvents like water, due to the presence of the amino and hydroxy groups, which can form hydrogen bonds.
  • Low Solubility in Non-Polar Solvents: Conversely, this compound may exhibit poor solubility in non-polar solvents like hexane or benzene, as the large diiodo-phenyl moiety increases its hydrophobic nature.
  • Effect of Temperature: Generally, increasing temperature can enhance solubility; however, specific studies would be required to determine the exact impact for this compound.
  • pH Influence: The solubility could also vary with pH, especially in acidic or basic environments where the amino group could become protonated or deprotonated, affecting solubility behavior.

In summary, the solubility behavior of methyl 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoate is governed by its dual nature, thereby making it more soluble in certain conditions while limiting its solubility in others. Analyzing solubility in the context of different solvents and environmental factors is crucial for understanding its practical applications.

Interesting facts

Interesting Facts about Methyl 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoate

Methyl 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoate, often referred to as a specific type of amino acid derivative, is an intriguing compound with various chemical and biological implications. Here are some fascinating insights regarding this compound:

  • Biological Relevance: This compound is a derivative of amino acids, which are the building blocks of proteins. It plays a role in biochemical pathways, particularly those involving neurochemicals.
  • Iodine Substituents: The presence of iodine in the structure, specifically in the form of diiodo substituents on the phenyl ring, significantly enhances the compound's *biological activity*. Iodine is known for its unique properties, often increasing the *lipophilicity* of organic molecules.
  • Potential Pharmaceutical Applications: Compounds with similar structures have been studied for their potential as *antimicrobial agents*. This may open doors for further research into their therapeutic properties.
  • Research Interest: The unique combination of an amino group and a phenolic hydroxyl group allows chemists to explore interesting reactions, such as nucleophilic attacks and the formation of versatile derivatives.
  • Structural Features: The compound exhibits a chiral center at the propanoate backbone, which means that it can exist in different isomeric forms. This property is critical in the field of *chiral synthesis*, where the specific isomer can exhibit distinct biological activities.

In summary, methyl 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoate stands out not only for its intricate structure but also for its potential applications in biological and medicinal chemistry. As researchers continue to investigate its properties, we may uncover even more about its capabilities and applications in the field of science.

Synonyms
SCHEMBL5797036
DB-080927