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3-Iodo-L-tyrosine

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Identification
Molecular formula
C9H10INO3
CAS number
70-78-0
IUPAC name
2-amino-2-(4-hydroxy-3-iodo-phenyl)acetic acid
State
State

This compound is generally found as a solid at room temperature.

Melting point (Celsius)
248.00
Melting point (Kelvin)
521.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
263.08g/mol
Molar mass
263.0780g/mol
Density
2.1400g/cm3
Appearence

3-Iodo-L-tyrosine typically appears as a white solid or powder. Its appearance may slightly vary depending on the degree of purity and specific form used.

Comment on solubility

Solubility of 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetic acid

The solubility of 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetic acid exhibits some intriguing characteristics that can be summarized as follows:

  • Polar Nature: The presence of both amino and hydroxy groups contributes to the compound's polar characteristics, enhancing its solubility in polar solvents like water.
  • Hydrogen Bonding: These functional groups allow for strong hydrogen bonding with water molecules, further facilitating dissolution.
  • Organic Solvents: While it is quite soluble in water, solubility may decrease in nonpolar organic solvents due to the hydrophobic interactions of the aromatic ring.
  • pH Dependency: The solubility can also be affected by the pH of the solution; at different pH levels, the ionization of the amino and hydroxy groups may change, enhancing or reducing solubility respectively.

In conclusion, it can be said that 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetic acid is generally soluble in aqueous environments, making it a compound that can effectively interact in biochemical processes. This property is essential for its potential applications in pharmaceuticals and biochemistry.

Interesting facts

Interesting Facts about 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetic acid

2-amino-2-(4-hydroxy-3-iodo-phenyl)acetic acid, often recognized for its diverse properties, is a compound of interest in both medicinal chemistry and biochemistry. Here are some key highlights about this intriguing substance:

  • Biological Significance: This compound is structurally related to amino acids and exhibits potential biological activity, particularly as a precursor for various pharmaceutical agents.
  • Antioxidant Properties: Due to the presence of the hydroxyl group, this compound may play a role as an antioxidant, helping to scavenge free radicals in biological systems.
  • Research Focus: Researchers are investigating its derivatives for applications in treating disorders such as cancer and neurodegenerative diseases.
  • Structure-Activity Relationship: The modification of both the amino and phenolic groups can significantly affect the compound’s pharmacological profile, making it a subject of extensive studies in drug design.
  • Potential for Synthesis: This compound serves as a valuable building block in organic synthesis, highlighting its versatility in creating more complex organic molecules.

As noted by one researcher, "The intricate balance between its molecular structure and biological activity presents a fascinating frontier for scientists in various fields." This reflects the compound's potential in advancing our understanding of small molecules in therapeutic applications.

In summary, 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetic acid not only demonstrates the complexity of amino acid analogs but also opens avenues for future research, contributing to the evolution of medicinal chemistry.

Synonyms
SCHEMBL20522819