1-(2-Hydroxyphenoxy)-1-deoxy-D-glucopyranose

Identification

Molecular formula

C₁₃H₁₈O₇

CAS number

.875548-23-9

IUPAC name

(2R,3R,4S,5S,6R)-6-[[2-(hydroxymethyl)phenoxy]methyl]tetrahydropyran-2,3,4,5-tetrol

State

At room temperature, this compound is solid. It is typically stable under normal conditions and is soluble in water, which is characteristic of many sugar analogues.

Melting point (Celsius)

120.50

Melting point (Kelvin)

393.65

Boiling point (Celsius)

313.20

Boiling point (Kelvin)

586.35

General information

Molecular weight

292.25g/mol

Molar mass

292.2540g/mol

Density

1.3700g/cm³

Appearence

The compound typically appears as a white to off-white crystalline powder. It is odorless and has a slightly sweet taste, resembling other sugar-related compounds.

Comment on solubility

Solubility of (2R,3R,4S,5S,6R)-6-[[2-(hydroxymethyl)phenoxy]methyl]tetrahydropyran-2,3,4,5-tetrol

The solubility of the compound (2R,3R,4S,5S,6R)-6-[[2-(hydroxymethyl)phenoxy]methyl]tetrahydropyran-2,3,4,5-tetrol, also known as a glycosylated tetrahydropyran derivative, exhibits some intriguing characteristics:

Polarity: Due to the presence of multiple hydroxyl (-OH) groups in its structure, the compound is likely to be highly polar. This generally leads to a higher solubility in polar solvents such as water.
Hydrophilic Interactions: The hydroxymethyl and phenoxy groups can engage in hydrogen bonding and dipole-dipole interactions, enhancing its solubility in aqueous solutions.
Solvent Dependence: While it can be soluble in water, its solubility may vary significantly in organic solvents. For example, it may have lower solubility in non-polar solvents owing to its structural characteristics.
Concentration Factors: The solubility will likely be influenced by temperature and concentration; higher temperatures may increase solubility, while the potential for aggregation at higher concentrations must be considered.

In conclusion, while the detailed solubility profile requires experimental determination, it is expected that this compound will be relatively soluble in polar solvents due to its multifunctional hydrophilic nature, likely providing opportunities for applications in various fields including pharmaceuticals and biochemistry.

Interesting facts

Exploring (2R,3R,4S,5S,6R)-6-[[2-(hydroxymethyl)phenoxy]methyl]tetrahydropyran-2,3,4,5-tetrol

The compound known as (2R,3R,4S,5S,6R)-6-[[2-(hydroxymethyl)phenoxy]methyl]tetrahydropyran-2,3,4,5-tetrol is a fascinating molecular structure with unique properties that make it an interesting subject for study in the field of organic chemistry. Here are some captivating facts about this compound:

Stereochemistry: The compound exhibits a complex stereochemistry, evidenced by its multiple chiral centers. This quality is crucial as it influences the compound's reactivity and interaction with biological systems.
Functional Groups: With an array of hydroxyl (-OH) and ether (R-O-R') functional groups, this compound can form hydrogen bonds, suggesting potential solubility in polar solvents and interactions with biomolecules.
Biological Relevance: The structural elements of this compound hint at possible biological activities. Many tetrahydropyrans and related compounds are known to exhibit pharmacological properties, including antimicrobial and anticancer effects.
Applications in Chemistry: Tetrahydropyran derivatives often find use in synthetic organic chemistry as building blocks for more complex molecules, especially in the synthesis of natural products and pharmaceuticals.
Research Opportunities: This compound presents intriguing avenues for research, including its potential as a scaffold for drug design, where modifications to the phenoxy group or hydroxymethyl moiety could yield new medicinal agents.

In summary, (2R,3R,4S,5S,6R)-6-[[2-(hydroxymethyl)phenoxy]methyl]tetrahydropyran-2,3,4,5-tetrol is not just noteworthy for its structure, but rather for its potential implications in organic synthesis and medicine. As with many compounds, the exploration of its properties can lead to significant advancements in both academic and applied chemistry.