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[2,3,4,5-tetrahydroxy-6-(p-tolylsulfonyloxy)hexyl] 4-methylbenzenesulfonate

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Identification
Molecular formula
C20H22O10S2
CAS number
108973-59-9
IUPAC name
[2,3,4,5-tetrahydroxy-6-(p-tolylsulfonyloxy)hexyl] 4-methylbenzenesulfonate
State
State

At room temperature, the compound exists in a solid state, typically as a crystalline powder. It is relatively stable in this form, though exposure to excessive moisture or heat may alter its state or appearance.

Melting point (Celsius)
115.00
Melting point (Kelvin)
388.15
Boiling point (Celsius)
264.00
Boiling point (Kelvin)
537.15
General information
Molecular weight
420.47g/mol
Molar mass
420.4720g/mol
Density
1.3520g/cm3
Appearence

The compound is a solid substance that often appears as a crystalline powder. It is typically colorless or may have a faint, off-white hue. Its appearance can vary slightly depending on the purity and specific sample preparation methods.

Comment on solubility

Solubility Characteristics

The compound [2,3,4,5-tetrahydroxy-6-(p-tolylsulfonyloxy)hexyl] 4-methylbenzenesulfonate exhibits intriguing solubility properties due to its complex structure, which incorporates multiple hydroxyl and sulfonate functional groups. These features significantly influence its interactions with solvents, particularly in polar environments.

Key Solubility Factors:

  • Hydroxyl Groups: The presence of four hydroxyl (-OH) groups contributes to the compound's ability to engage in hydrogen bonding, which generally enhances solubility in polar solvents such as water.
  • Sulfonate Group: The sulfonate moiety (-SO3-) is highly polar and hydrophilic, further promoting solubility in aqueous solutions and making the compound more suited for biological interactions.
  • Hydrophobic Regions: The p-tolyl group introduces a hydrophobic element, which may limit solubility in non-polar solvents, causing a preference for polar environments.

Overall, the solubility of this compound can be summarized as follows:

  • Soluble in polar solvents (e.g., water, alcohols)
  • Limited solubility in non-polar solvents (e.g., hexane, toluene)

In summary, the solubility of [2,3,4,5-tetrahydroxy-6-(p-tolylsulfonyloxy)hexyl] 4-methylbenzenesulfonate is enhanced by its polar functional groups, making it particularly effective in environments where polar interactions are essential. This property is crucial for its potential applications in chemical and biochemical contexts.

Interesting facts

Interesting Facts about [2,3,4,5-Tetrahydroxy-6-(p-tolylsulfonyloxy)hexyl] 4-Methylbenzenesulfonate

This compound, known for its complex structure, is a prime example of the intricate world of organic chemistry. It offers a multitude of interesting aspects worth exploring:

  • Functional Diversity: The presence of multiple hydroxyl (-OH) groups plays a critical role in the compound's chemical reactivity. These groups can act as nucleophiles in many organic reactions, enhancing its versatility in synthetic pathways.
  • Sulfonyloxy Group: The incorporation of the p-tolylsulfonyloxy group contributes to the compound’s potential as a leaving group in nucleophilic substitution reactions. As a result, it can be utilized effectively in various chemical transformations.
  • Biological Potential: Compounds with this structural configuration often exhibit significant biological activity. They may serve as intermediates in the synthesis of pharmaceuticals or as agents in biochemical reactions, making them a focus of ongoing research.
  • Stereochemistry: The tetrahydroxy configuration introduces stereochemical variability, allowing for the exploration of enantiomeric forms of the compound. Such diversity can lead to differing biological activities, a subject of immense interest in medicinal chemistry.
  • Organic Synthesis Applications: Given its structural characteristics, this compound can be employed as a starting material in the synthesis of more complex molecules, facilitating advancements in organic synthesis methodologies.

As a remarkable compound with a unique configuration, [2,3,4,5-tetrahydroxy-6-(p-tolylsulfonyloxy)hexyl] 4-methylbenzenesulfonate stands at the confluence of organic chemistry and biological exploration. Its intricate design is not just a testament to the art of molecular architecture but also to the potential for innovation in application and synthesis.

Synonyms
DTXSID80950993
1,6-Bis-O-(4-methylbenzene-1-sulfonyl)hexitol
RefChem:1053490
DTXCID701379128
1,6-Ditosyl-D-mannitol
28296-02-8
1,6-Bis(p-toluenesulfonyl)-D-mannitol
D-MANNITOL, 1,6-BIS(p-TOLUENESULFONATE)