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2-methyl-6-(2-nitrophenoxy)tetrahydropyran-3,4,5-triol

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Identification
Molecular formula
C12H15NO6
CAS number
156765-75-0
IUPAC name
2-methyl-6-(2-nitrophenoxy)tetrahydropyran-3,4,5-triol
State
State

At room temperature, this compound is usually found in a solid state due to its molecular structure and relatively high molecular weight. Given its crystalline texture, it is stable under standard conditions but may require careful handling if in powdered form to prevent inhalation or exposure.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.15
Boiling point (Celsius)
355.00
Boiling point (Kelvin)
628.15
General information
Molecular weight
287.27g/mol
Molar mass
287.2740g/mol
Density
1.4200g/cm3
Appearence

The compound is typically a pale yellow crystalline substance, indicative of many nitroaromatic compounds. It can be sensitive to light, leading to gradual discoloration if not stored properly. It has a fibrous texture due to its crystalline nature, and can be powdery when ground.

Comment on solubility

Solubility of 2-methyl-6-(2-nitrophenoxy)tetrahydropyran-3,4,5-triol

The solubility of 2-methyl-6-(2-nitrophenoxy)tetrahydropyran-3,4,5-triol (C12H15NO6) is influenced by its molecular structure and functional groups. This compound contains both hydrophilic (water-attracting) and hydrophobic (water-repelling) regions, which play a crucial role in its solubility behavior.

Factors Affecting Solubility:

  • Polarity: The presence of multiple hydroxyl groups (-OH) enhances the polarity of the molecule, making it more likely to dissolve in polar solvents such as water.
  • Hydrogen Bonding: The ability of the hydroxyl groups to form hydrogen bonds contributes significantly to its solubility in aqueous solutions.
  • Substituents: The 2-nitrophenoxy group introduces additional polarity, but the overall effects on solubility will depend on the balance between the hydrophilic and hydrophobic portions of the molecule.
  • Concentration: In practical applications, solubility can vary with concentration; lower concentrations may lead to different solubilization dynamics than higher concentrations.

In summary, while 2-methyl-6-(2-nitrophenoxy)tetrahydropyran-3,4,5-triol is expected to exhibit reasonable solubility in polar solvents due to its hydrophilic functional groups, external factors such as temperature, pH, and the presence of other solutes can further influence its solubility characteristics.

Interesting facts

Interesting Facts about 2-methyl-6-(2-nitrophenoxy)tetrahydropyran-3,4,5-triol

This fascinating compound, known as 2-methyl-6-(2-nitrophenoxy)tetrahydropyran-3,4,5-triol, can be viewed as a promising subject of study in the realms of chemistry and pharmaceuticals. Below are some compelling aspects of this compound:

  • Functional Diversity: The presence of multiple functional groups, including a nitrophenyl ring and multiple hydroxyl groups, illustrates the compound's versatility, making it an interesting candidate for chemical reactions and synthesis.
  • Potential Biological Activity: Compounds with nitro groups are often known for their significant biological activities. The inclusion of a nitrophenyl moiety can suggest potential antibacterial or anticancer properties, making this compound a subject of interest in medicinal chemistry.
  • Synthetic Routes: The synthesis of compounds like this one often involves advanced techniques in organic chemistry, such as hydrogenation and substitution reactions. Students and researchers can explore various synthetic pathways to create this compound, enhancing their laboratory skills.
  • Structure-Activity Relationship (SAR): Due to its unique structure, this compound offers opportunities to study the structure-activity relationships. Understanding how variations in structure can affect its biological function can lead to the design of more effective drugs.
  • Role of Tetrahydropyran: The tetrahydropyran ring contributes to the compound's stability and reactivity. This six-membered cyclic ether is known for its unique conformational properties and can impact the overall behavior of the compound in various environments.
  • Environmental Relevance: Investigating the environmental fate of such nitro compounds is also crucial, as they may undergo transformations that impact their toxicity and biodegradability. This aspect is vital for chemical safety and regulatory considerations.

In summary, 2-methyl-6-(2-nitrophenoxy)tetrahydropyran-3,4,5-triol is not just a chemical entity but a portal to understanding deeper principles in organic chemistry and pharmacology. As scientists unravel the complexities surrounding this compound, they can contribute to developing new technologies and therapeutics that push the boundaries of science.

Synonyms
2-nitrophenyl 6-deoxyhexopyranoside
150025-35-7
PNP-beta-D-FUC
O-Nitrophenyl b-D-fucopyranoside
2-Nitrophenyl-beta-D-fucopyranoside
2-Nitrophenyl beta -D-fucopyranoside
AKOS030241589
2-Nitrophenyl beta-D-fucopyranoside, >=99% (TLC)