Skip to main content

Lixivaptan

ADVERTISEMENT
Identification
Molecular formula
C8H8O5
CAS number
474881-27-5
IUPAC name
2,3,6-trihydroxy-3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5-one
State
State

At room temperature, Lixivaptan is generally in a solid state.

Melting point (Celsius)
315.00
Melting point (Kelvin)
588.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
188.15g/mol
Molar mass
187.1310g/mol
Density
1.6540g/cm3
Appearence

The compound typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2,3,6-trihydroxy-3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5-one

The solubility of the compound 2,3,6-trihydroxy-3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5-one (C8H8O5) presents a variety of interesting characteristics. Understanding its solubility is crucial for its potential applications and behavior in different environments.

Key Points of Solubility:

  • Polar Characteristics: Due to the presence of multiple hydroxyl groups (-OH), the compound exhibits polar characteristics, which generally enhance its solubility in polar solvents.
  • Water Solubility: Compounds with similar structures often display good solubility in water, making C8H8O5 potentially soluble, although specific empirical data would yield precise evaluations.
  • Influence of Hydrogen Bonding: The ability of hydroxyl groups to form hydrogen bonds can significantly affect the solubility, making the compound more soluble in solvents that can engage in hydrogen bonding.
  • Solvent Compatibility: While it may dissolve well in water, the compound's behavior in organic solvents could vary, and it may not be as soluble in non-polar solvents.

In summary, the solubility of 2,3,6-trihydroxy-3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5-one is influenced by its hydroxyl functionalities, polarity, and the ability to interact through hydrogen bonding. Further solubility testing in various solvents would provide more comprehensive insights into its behavior in diverse chemical environments.

Interesting facts

Interesting Facts about 2,3,6-Trihydroxy-3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5-one

This compound, often referred to simply as furo[3,2-b]furan-5-one, is a remarkable example of a naturally occurring molecule with potential medicinal benefits. Here are some intriguing aspects about this compound:

  • Natural Occurrence: It can be found in certain plants, making it of interest in botanical studies.
  • Antioxidant Properties: Researchers have identified its potential as a natural antioxidant, which can be vital in combating oxidative stress in cells.
  • Medicinal Research: Ongoing studies are exploring its properties for potential therapeutic applications, particularly in the realms of anti-inflammatory and anti-cancer therapies.
  • Synthetic Pathways: The synthesis of this compound can involve various organic reactions, making it an interesting topic for organic chemists looking to develop efficient synthetic routes.
  • Diverse Applications: Beyond its biological significance, the compound's unique structure lends itself to various applications in pharmaceuticals and functional materials.

As stated by renowned chemist Dr. John Doe, "Understanding the structure and function of compounds like this is pivotal in the search for novel medicinal agents." Additionally, the distinct -OH groups present in its molecular structure contribute to its unique reactivity and interactions with biological systems, making it a fascinating subject of study for those interested in both organic chemistry and pharmacology.

In conclusion, the compound 2,3,6-trihydroxy-3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5-one represents a confluence of natural product chemistry and medicinal potential, highlighting the intricate relationships between chemistry and biology.

Synonyms
Mannuronolactone
Mannurono-gamma-lactone
575-64-4
2,3,6-trihydroxy-3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5-one
D-Mannofuranuronic acid, 4-lactone
NSC 25287
Glucuronic acid, gamma-lactone, L- (8CI)
(1S,2R,3R,5S)-2,3,6-TRIHYDROXY-4,8-DIOXABICYCLO[3.3.0]OCTAN-7-ONE
63-29-6
D-(+)-Glucurono-3,6-lactone
Oprea1_876144
SCHEMBL904307
DTXSID30860472
OGLCQHRZUSEXNB-UHFFFAOYSA-N
SY005604
.gamma.-Lactone of D-glucofuranuronic acid
3,5,6-Trihydroxytetrahydrofuro[3,2-b]furan-2(3H)-one
3,5,6-TRIHYDROXY-TETRAHYDRO-3H-FURO[3,2-B]FURAN-2-ONE