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Calycanthoside

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Identification
Molecular formula
C11H17NO7
IUPAC name
2-(4-aminophenoxy)-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol
State
State

At room temperature, calycanthoside exists as a solid in the form of crystalline powder.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
285.27g/mol
Molar mass
285.2740g/mol
Density
1.5800g/cm3
Appearence

Calycanthoside generally appears as a colorless to pale-yellow crystalline powder. It is typically odorless and has a slightly bitter taste.

Comment on solubility

Solubility of 2-(4-aminophenoxy)-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

The compound 2-(4-aminophenoxy)-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol, with the chemical formula C11H17NO7, exhibits intriguing solubility characteristics that can be influenced by several factors.

Key Points on Solubility:

  • Polarity: The presence of multiple hydroxyl (-OH) groups contributes to the overall polarity of the molecule, which enhances its potential for solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds is particularly significant. The hydroxymethyl groups provide active sites for hydrogen bonding, which can facilitate solvation in aqueous environments.
  • Structure: The complex tetrahydropyran ring structure can affect the steric hindrance and the accessibility of these functional groups, further influencing solubility behavior.
  • Temperature Dependence: The solubility may vary with temperature, as increasing temperature often enhances solubility for many organic compounds, including those with polar nature.

Overall, while the presence of functional groups suggests a potential for reasonable solubility in polar solvents, empirical testing is essential to determine the exact solubility characteristics in various conditions. As such, solubility can be considered a multifaceted property that depends on both molecular structure and environmental factors.

Interesting facts

Interesting Facts About 2-(4-aminophenoxy)-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

This compound, commonly referred to in scientific literature for its intriguing chemical structure, possesses unique characteristics that make it a subject of interest for researchers:

  • Biological Significance: The presence of both amino and hydroxymethyl groups in its structure suggests potential biological activity. Compounds like this often play roles in biochemistry and medicinal chemistry, acting as pharmacophores in drug discovery.
  • Structural Diversity: This molecule is a prime example of a complex heterocyclic compound. Heterocycles are crucial in medicinal chemistry as they can improve the solubility and bioavailability of drugs.
  • Potential Applications: Given its multi-functional groups, this compound may have applications in creating targeted therapies or novel materials. Its ability to interact with biological systems makes it a potential candidate for further studies in drug formulation.
  • Chemical Robustness: The tetrahydropyran ring provides structural stability, which is essential for maintaining efficacy during metabolic processes in living organisms.
  • Research Treasures: Compounds like 2-(4-aminophenoxy)-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol often serve as intermediates or building blocks in the synthesis of more complex molecules, enriching the field of organic synthesis.

In summary, the unique structure and functional groups of this compound contribute to its potential diversity in applications, making it a fascinating topic for ongoing research in both synthesis and biological evaluations. As stated, "Chemistry is the art of transformation," and this compound exemplifies that art through its versatile properties.

Synonyms
(2R,3R,4S,5S,6R)-2-(4-aminophenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
2-(4-aminophenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
31302-52-0
4-Aminophenyl ?-D-Galactopyranoside
p-aminophenyl-hexopyranoside
SCHEMBL4760031
SCHEMBL22021911
p-Aminophenyl b-D-glucopyranoside
4-Aminophenyl-b-D-galactopyranoside
NSC87909
GLUCOPYRANOSIDE,4-AMINOPHENYL
NSC-87909
AKOS032947929
SB49600
LS-14107
SR-01000883736
SR-01000883736-1
4-Aminophenyl beta-D-galactopyranoside, beta-galactosidase substrate