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Cyclotetrametamycin

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Identification
Molecular formula
C8H12O5
CAS number
52212-06-5
IUPAC name
(2R,3R,4S)-3-hydroxy-2,3,4-trimethyl-5-oxo-tetrahydrofuran-2-carboxylic acid
State
State

At room temperature, (2R,3R,4S)-3-hydroxy-2,3,4-trimethyl-5-oxo-tetrahydrofuran-2-carboxylic acid is a solid. It is typically handled in its crystalline powder form in laboratory settings.

Melting point (Celsius)
154.00
Melting point (Kelvin)
427.15
Boiling point (Celsius)
285.20
Boiling point (Kelvin)
558.35
General information
Molecular weight
186.18g/mol
Molar mass
186.1790g/mol
Density
1.3540g/cm3
Appearence

The compound is typically observed as a white crystalline powder. It may display slight variations in color based on the purity and the environmental conditions, but it generally retains a consistent solid appearance under standard lab conditions.

Comment on solubility

Solubility of (2R,3R,4S)-3-hydroxy-2,3,4-trimethyl-5-oxo-tetrahydrofuran-2-carboxylic acid

The solubility of (2R,3R,4S)-3-hydroxy-2,3,4-trimethyl-5-oxo-tetrahydrofuran-2-carboxylic acid can be influenced by several factors such as temperature, pH, and the presence of other solutes.

Key considerations for its solubility include:

  • Functional Groups: The presence of carboxylic acid groups contributes to increased solubility in polar solvents, particularly in water.
  • Hydrogen Bonding: The hydroxy group enhances the ability to form hydrogen bonds with water, thus promoting solubility.
  • Chain Flexibility: The presence of a tetrahydrofuran ring provides some rigidity, which may impact the overall solubility profile.

In general, compounds featuring both polar and non-polar characteristics can exhibit interesting solubility behavior, often described as “like dissolves like.” Therefore:

  • Water: Likely soluble due to hydrogen bonding and polar character.
  • Non-Polar Solvents: Less likely to dissolve due to the absence of favorable interactions.

In conclusion, the solubility of this compound is expected to be significant in aqueous environments, influenced by its unique structural attributes. This illustrates the intricate relationship between molecular structure and solubility, highlighting the importance of chemical properties in solution dynamics.

Interesting facts

Interesting Facts about (2R,3R,4S)-3-hydroxy-2,3,4-trimethyl-5-oxo-tetrahydrofuran-2-carboxylic Acid

(2R,3R,4S)-3-hydroxy-2,3,4-trimethyl-5-oxo-tetrahydrofuran-2-carboxylic acid, often simply referred to as a complex cyclic compound, offers a fascinating glimpse into the world of organic chemistry and its applications. Here are some key points that highlight its significance:

  • Stereochemistry: This compound exhibits a specific stereochemical configuration, which plays a crucial role in its reactivity and interaction with biological systems. The arrangement of its R and S centers defines its properties.
  • Functional Groups: The presence of hydroxyl (-OH) and carboxylic acid (-COOH) functional groups confers unique chemical reactivity, enabling it to participate in various biochemical processes.
  • Potential Applications: Compounds of this nature may have potential in medicinal chemistry, particularly in the design of new drugs that target specific biological pathways, due to their structural complexity.
  • Natural Products: Many complex cyclic compounds are derived from natural sources, and this one may also be related to natural metabolites, showcasing the connection between organic synthesis and natural chemistry.
  • Research Significance: Understanding such compounds can lead to insights into synthetic methodologies, allowing chemists to develop more efficient ways to create similar structures in the lab.

In summary, (2R,3R,4S)-3-hydroxy-2,3,4-trimethyl-5-oxo-tetrahydrofuran-2-carboxylic acid not only fascinates with its intricate structure but also holds potential for exciting discoveries in both research and practical applications. As chemists continue to explore the depths of such compounds, the possibilities are truly endless.

Synonyms
RefChem:1089823
Monocrotalic acid
2-Furoic acid, tetrahydro-3-hydroxy-2,3,4-trimethyl-5-oxo-, (2R,3R,4R)-
2-Furancarboxylic acid, tetrahydro-3-hydroxy-2,3,4-trimethyl-5-oxo-, (2R-(2-alpha,3-beta,4-alpha))-