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3R,4R,5R-4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol

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Identification
Molecular formula
C25H30O6
CAS number
n/a
IUPAC name
(3R,4R,5R)-4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol
State
State
At room temperature, the compound is typically a liquid, but it may also crystallize into a solid state under certain conditions.
Melting point (Celsius)
22.00
Melting point (Kelvin)
295.15
Boiling point (Celsius)
161.00
Boiling point (Kelvin)
434.15
General information
Molecular weight
442.55g/mol
Molar mass
442.5510g/mol
Density
1.1752g/cm3
Appearence

The compound typically appears as a clear colorless to light yellow liquid with a pleasant odor, due to the presence of benzyl groups. It may also appear in the form of a white crystalline solid when purified.

Comment on solubility

Solubility of (3R,4R,5R)-4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol

The solubility of the compound (3R,4R,5R)-4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol is influenced by its complex molecular structure and the presence of various functional groups. Understanding its solubility characteristics can be crucial for its applications in both laboratory and industrial settings. Here are some key points regarding its solubility:

  • General Solubility: This compound's solubility in water is expected to be relatively low due to its large hydrophobic aromatic groups (benzyloxy and dibenzyloxy) which do not favor interaction with polar solvents.
  • Organic Solvents: It is likely to exhibit better solubility in non-polar or slightly polar organic solvents, such as ethanol, methanol, and chloroform, where its hydrophobic regions can interact more favorably.
  • Temperature Effects: Increasing the temperature generally enhances solubility in organic solvents, which may be beneficial during synthesis and extraction processes.
  • Miscibility: When mixed with other compounds, solubility behaviors could vary, highlighting the importance of checking the mutual solubility with other solvent systems in practical applications.

In conclusion, while the solubility profile of (3R,4R,5R)-4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol presents some challenges, its behavior in organic solvents opens up avenues for effective usage in synthesis and formulation endeavors.

Interesting facts

Interesting Facts about (3R,4R,5R)-4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol

The compound (3R,4R,5R)-4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol is a fascinating example of a complex organic molecule that showcases some important features of stereochemistry and functional group diversity. Here are some intriguing aspects about this compound:

  • Stereochemical Complexity: The presence of multiple chiral centers in its structure means it can exist in different stereoisomeric forms. This makes it an interesting subject for studies on enantioselectivity and molecular behavior in biological systems.
  • Functional Groups: This molecule incorporates a variety of functional groups such as ethers and alcohols, which can influence its reactivity, solubility, and interactions with other molecules. The benzyloxy groups provide interesting characteristics such as potential for selective cleavage in synthetic pathways.
  • Potential Applications: Due to its structure, it may serve as a building block in the synthesis of larger, biologically active compounds. Compounds with furan rings are often investigated for their medicinal properties, including antimicrobial and anti-inflammatory activities.
  • History of Research: Compounds derived from tetrahydrofuran scaffolds have been extensively studied for their role in natural product synthesis. This makes them relevant in both academic and pharmaceutical research.
  • Natural Analogues: The molecular design is reminiscent of many natural substances, giving it a potential role in mimicking or enhancing the activity of certain natural compounds.

This compound exemplifies the complexity and beauty of organic chemistry, illustrating how detailed structures can lead to diverse functionalities and interactions. Its study can contribute to advancements in various fields including organic synthesis, pharmacology, and materials science.

Synonyms
Tribenoside (JAN/USAN/INN)
SCHEMBL1652290
CHEBI:32256
AKOS015896834
D01095