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Boc-5-(2-phenylacetyl)oxyamino-pentylammonium chloride

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Identification
Molecular formula
C20H27ClN2O4
CAS number
87680-60-4
IUPAC name
[(1S)-1-benzyloxycarbonyl-5-[(2-phenylacetyl)oxyamino]pentyl]ammonium;chloride
State
State

At room temperature, Boc-5-(2-phenylacetyl)oxyamino-pentylammonium chloride is in a solid state. It is usually handled as a powder.

Melting point (Celsius)
140.00
Melting point (Kelvin)
413.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
377.92g/mol
Molar mass
377.9240g/mol
Density
1.2200g/cm3
Appearence

The compound appears as a white crystalline powder. It is typically provided in a stable form and is sensitive to moisture.

Comment on solubility

Solubility of [(1S)-1-benzyloxycarbonyl-5-[(2-phenylacetyl)oxyamino]pentyl]ammonium;chloride

The solubility of [(1S)-1-benzyloxycarbonyl-5-[(2-phenylacetyl)oxyamino]pentyl]ammonium;chloride can be influenced by several factors, making it an intriguing compound to study. Here are some key points about its solubility:

  • Solvent Type: This compound is likely to be more soluble in polar solvents, such as water or methanol, due to the presence of ammonium functional groups that interact favorably with polar molecules.
  • pH Dependence: The solubility may also be pH-dependent. As an ammonium salt, its solubility in water could vary with changes in pH, possibly increasing in acidic conditions.
  • Temperature Effects: Increased temperature generally enhances solubility; therefore, warming the solvent might improve the compound's dissolution.
  • Presence of Ionic Species: The solubility could be affected by the presence of other ionic species in solution, which might either stabilize or destabilize the compound.

In conclusion, while specific experimental data would provide a more accurate depiction of solubility, the structural characteristics hint that the compound should exhibit reasonable solubility in appropriate solvents, especially those that are polar. Understanding the factors that affect its solubility is essential for applications in chemical and pharmaceutical contexts.

Interesting facts

Interesting Facts About [(1S)-1-benzyloxycarbonyl-5-[(2-phenylacetyl)oxyamino]pentyl]ammonium;chloride

This compound represents a fascinating intersection of organic synthesis and medicinal chemistry. Here are some key points to pique your interest:

  • Biological Applications: The structural components of this compound suggest potential uses in drug design, particularly in the development of new therapeutic agents. Its unique structure may help facilitate interactions with biological targets.
  • Ammonium Functionality: The presence of the ammonium group is of particular interest. Compounds with ammonium functionalities often display interesting properties as cationic surfactants, which can enhance solubility and stability in biological systems.
  • Carbamate Linkages: The benzyloxycarbonyl (Z) protecting group is widely utilized in peptide synthesis. It allows for selective deprotection, making it invaluable in generating complex peptide structures.
  • Amino Acid Analog: This compound can be viewed as an amino acid analog, which opens up avenues for studying its interactions with amino acid transporters and potential roles in signaling pathways.
  • Chloride Counterion: The chloride ion as a counterion plays a crucial role in the stability and solubility of this compound, essential for its effective use in various chemical and biochemical applications.

This compound not only embodies the creativity inherent in synthetic organic chemistry but also highlights the ongoing exploration of new materials and drugs that can impact human health. As scientists continue to investigate its properties and reactions, we stand on the brink of uncovering novel uses and applications yet to be discovered!

Synonyms
Benzyl N6-benzyloxycarbonyl-L-lysinate hydrochloride
EINECS 228-859-9
DTXSID90274733
NSC 88180
Lysine, N(6)-carboxy-, dibenzyl ester, hydrochloride, L-
N-epsilon-Carbobenzyloxy-L-lysine benzyl ester hydrochloride
LYSINE, N(sup 6)-(PHENYLACETOXY)-, BENZYL ESTER, MONOHYDROCHLORIDE, L-
L-Lysine, N(6)-((phenylmethoxy)carbonyl)-, phenylmethyl ester, monohydrochloride
73747-57-6
DTXCID50226192
Lysine, N(6)-carboxy-, dibenzyl ester, hydrochloride, L-(8CI)
L-Lysine, N(6)-((phenylmethoxy)carbonyl)-, phenylmethyl ester, monohydrochloride (9CI)
228-859-9