Skip to main content

Not Available

ADVERTISEMENT
Identification
Molecular formula
C28H32O6
CAS number
: Not Available
IUPAC name
4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol
State
State

The state of this compound at room temperature is not well-documented. However, compounds of similar structure can be solids or oils at room temperature, often dependent on the specific substitutions and their arrangement.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
448.55g/mol
Molar mass
0.0000g/mol
Density
0.0000g/cm3
Appearence

There is no available standard information on the appearance of this specific compound, as it is a complex organic molecule and not commonly referenced outside of specific chemical synthesis contexts. However, similar types of compounds are often viscous oils or crystalline solids, depending on their exact configuration and state of purification.

Comment on solubility

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

The solubility of the compound 4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol (C28H32O6) can vary significantly depending on several factors including solvent choice, temperature, and molecular interactions. Here are some key points to consider:

  • Hydrophobic Character: This compound contains multiple aromatic rings and long alkyl chains which may contribute to its hydrophobic nature.
  • Polar Groups: The presence of hydroxyl (-OH) and ethoxy (-OEt) groups enhances its potential for hydrogen bonding, which can increase its solubility in polar solvents.
  • Solvent Compatibility: It is expected to be more soluble in organic solvents such as ethanol, methanol, or dichloromethane compared to water due to its structural characteristics.
  • Temperature Influence: Higher temperatures generally increase the solubility of organic compounds; thus, moderate heating may help to dissolve this compound better in selected organic solvents.

In summary, while the solubility of this compound in water may be limited due to its hydrophobic segments, its solubility in organic solvents is likely enhanced by the presence of polar functional groups. Understanding these factors is crucial for practical applications in chemical synthesis and formulation.

Interesting facts

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

The compound 4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol is a fascinating molecule that showcases the complexity and creativity inherent in organic chemistry. It belongs to a class of compounds known as tetrahydrofuran derivatives, which are noteworthy due to their unique cyclic structure and functional groups.

Key Features:

  • Structural Complexity: Its intricate structural arrangement makes it a valuable subject of study in synthetic organic chemistry.
  • Potential Applications: Tetrahydrofuran derivatives are often investigated for their potential therapeutic effects and applications in the pharmaceutical industry.
  • Diverse Functional Groups: The presence of multiple functional groups, such as ether and alcohol, suggests that this compound could participate in various chemical reactions, serving as a versatile building block in organic synthesis.
  • Synthetic Intermediates: This compound can likely be used as an intermediate in the synthesis of more complex molecules, highlighting its importance in drug design and development.

It's noteworthy that compounds like this demonstrate the significance of regioselectivity and stereochemistry in organic synthesis. In the words of chemists, “The beauty of organic chemistry lies in the structure-function relationship.” This statement holds true as the structural features of 4-benzyloxy-5-(1,2-dibenzyloxyethyl)-2-ethoxy-tetrahydrofuran-3-ol can influence its chemical reactivity and interaction with biological systems.

As a chemistry student or a budding chemist, understanding such compounds enriches your appreciation for the molecular diversity present in the chemistry world. You’ll find that exploring such structures opens doors to new discoveries and innovative applications in various fields.

Synonyms
Glyvenol
SCHEMBL637603
Ethyl 3,5,6-tri-O-benzyl-D-glucofuranoside;Ethyl 3,5,6-tri-O-benzyl-D-glucofuranoside
(3R,4R,5R)-5-[1,2-bis(phenylmethoxy)ethyl]-2-ethoxy-4-phenylmethoxyoxolan-3-ol