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Boc-Lys(Z)-OH

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Identification
Molecular formula
C25H27NO3
CAS number
37538-61-5
IUPAC name
2-[(4,4-diphenylcyclohexyl)-(2-hydroxyethyl)amino]ethanol
State
State

At room temperature, this compound typically exists in a solid state.

Melting point (Celsius)
131.50
Melting point (Kelvin)
404.65
Boiling point (Celsius)
472.70
Boiling point (Kelvin)
745.85
General information
Molecular weight
397.50g/mol
Molar mass
397.5650g/mol
Density
1.1460g/cm3
Appearence

The compound is generally a white or off-white solid and is frequently used in chemical derivatization and as a protecting group for amino acids.

Comment on solubility

Solubility of 2-[(4,4-diphenylcyclohexyl)-(2-hydroxyethyl)amino]ethanol

The solubility of 2-[(4,4-diphenylcyclohexyl)-(2-hydroxyethyl)amino]ethanol is influenced by various factors owing to its complex structure. Generally speaking, the solubility of this compound can be characterized as follows:

  • Polar and Non-Polar Characteristics: With a hydroxyethyl functional group, this compound displays both polar and non-polar characteristics, potentially leading to solubility in a range of solvents.
  • Aqueous Solubility: The presence of the hydroxyl group makes it moderately soluble in water, although the large hydrophobic cyclohexyl groups may impede extensive solubility.
  • Organic Solvents: It is likely to have higher solubility in organic solvents such as ethanol, methanol, or acetone, which can stabilize the compound’s non-polar characteristics.
  • pH Dependence: Depending on the pH of the solution, the solubility can vary significantly, particularly due to the amine group which can accept protons under acidic conditions.

In practical applications, the solubility profile of 2-[(4,4-diphenylcyclohexyl)-(2-hydroxyethyl)amino]ethanol should be considered for its potential use in pharmaceuticals, where effective solubility is crucial. Overall, while some solubility can be expected, it is often moderate and context-dependent.

Interesting facts

Interesting Facts about 2-[(4,4-diphenylcyclohexyl)-(2-hydroxyethyl)amino]ethanol

This intriguing compound, often referred to in the scientific community as a member of the family of amino alcohols, possesses unique characteristics and applications that make it noteworthy. Here are some fascinating points to consider:

  • Pharmaceutical Application: This compound is studied for its potential use in medicinal chemistry, particularly in the development of drugs that target nervous system disorders.
  • Synthetic Pathway: Its synthesis typically involves multi-step organic reactions, showcasing the complexity of constructing compounds with multiple functional groups.
  • Structure-Activity Relationship (SAR): The specific arrangement of the diphenylcyclohexyl and hydroxyethyl groups contributes to its biological activity, making it a subject of SAR studies.
  • Binding Affinity: Research indicates that it may have the ability to interact with specific receptors in the brain, potentially influencing neurotransmitter systems.
  • Solubility Profiles: As an amino alcohol, the compound's amphiphilic nature allows it to participate in both hydrophilic and hydrophobic interactions, which is crucial for its biological functions.

Additionally, this compound exemplifies the intricate relationship between molecular structure and function, making it an exciting area of study for both chemists and pharmacologists. As one researcher noted, "Understanding these connections can lead to breakthroughs in drug design." The exploration of 2-[(4,4-diphenylcyclohexyl)-(2-hydroxyethyl)amino]ethanol continues to inspire new insights into medicinal applications.

Synonyms
A36KC267MG
2,2'-[(4,4-Diphenylcyclohexyl)imino]bis[ethanol]
Ethanol, 2,2'-[(4,4-diphenylcyclohexyl)imino]bis-
742631-64-7