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Benzyloxycarbonyltyrosine

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Identification
Molecular formula
C17H17NO5
CAS number
1145-60-4
IUPAC name
2-amino-3-(4-benzyloxycarbonyloxyphenyl)propanoic acid
State
State

At room temperature, benzyloxycarbonyltyrosine is in a solid state, typically as a crystalline powder.

Melting point (Celsius)
123.00
Melting point (Kelvin)
396.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
299.31g/mol
Molar mass
299.3130g/mol
Density
1.3320g/cm3
Appearence

Benzyloxycarbonyltyrosine typically appears as a white to off-white crystalline powder. Its physical state can vary slightly based on purity and preparation methods, but it is generally uniform in texture and color.

Comment on solubility

Solubility of 2-amino-3-(4-benzyloxycarbonyloxyphenyl)propanoic acid (C17H17NO5)

The solubility of 2-amino-3-(4-benzyloxycarbonyloxyphenyl)propanoic acid is influenced by its unique structural features. This compound contains both hydrophilic and hydrophobic components, making it an intriguing subject for solubility studies.

  • It exhibits a moderate solubility in water, largely due to the presence of the amino group (–NH2) which can form hydrogen bonds with water molecules.
  • The benzyloxycarbonyloxyphenyl moiety contributes to its hydrophobic character, thus limiting its solubility in aqueous environments.
  • As with many organic compounds, solubility may increase in polar organic solvents such as methanol or ethanol.

In conclusion, while 2-amino-3-(4-benzyloxycarbonyloxyphenyl)propanoic acid has some degree of solubility in water, its overall solubility characteristics are dictated by a balance between its hydrophilic and hydrophobic segments, emphasizing the importance of molecular structure in determining solubility behavior.

Interesting facts

Interesting Facts about 2-amino-3-(4-benzyloxycarbonyloxyphenyl)propanoic acid

2-amino-3-(4-benzyloxycarbonyloxyphenyl)propanoic acid, often abbreviated as (Boc)2-aminoproprionate, belongs to a class of compounds known as amino acids. Here are some engaging aspects of this intriguing compound:

  • Amphoteric Nature: Like many amino acids, this compound exhibits both acidic and basic properties, allowing it to act as a zwitterion in certain environments. This behavior is essential for its role in biological systems.
  • Pharmaceutical Relevance: Compounds similar to this amino acid are investigated for their potential use in drug design. Their structural variants can lead to the development of innovative therapeutic agents, particularly in the fields of neurobiology and oncology.
  • Functional Group Diversity: The presence of the benzyloxycarbonyl (Boc) moiety enhances the compound's reactivity, making it a valuable intermediate in organic synthesis. This functional diversity is useful in developing more complex molecules.
  • Research Applications: Researchers often utilize derivatives of amino acids like this compound in the study of peptide synthesis and protein folding. This contributes significantly to our understanding of biochemistry and molecular biology.
  • Environmental Impact: Amino acids play vital roles in various biological cycles and can have applications in sustainable agricultural practices as well as environmental biotechnology, where they aid in the biodegradation of pollutants.

In summary, 2-amino-3-(4-benzyloxycarbonyloxyphenyl)propanoic acid is not just a simple molecule; it embodies a wealth of potential applications and importance that highlights its significance in both chemistry and biology. Exploring its properties and reactions can lead to exciting discoveries in both research and industry.

Synonyms
O-Z-L-tyrosine
(2S)-2-amino-3-(4-phenylmethoxycarbonyloxyphenyl)propanoic acid
O-[(Phenylmethoxy)carbonyl]-L-tyrosine
NSC88500
NCIOpen2_009647
2-amino-3-(4-phenylmethoxycarbonyloxyphenyl)propanoic acid
NSC-88500