Interesting facts
Interesting Facts about (3R,4R,5R,6S)-6-methyltetrahydropyran-2,3,4,5-tetrol
(3R,4R,5R,6S)-6-methyltetrahydropyran-2,3,4,5-tetrol is a captivating organic compound notable for its intricate stereochemistry and functional groups. Here are some fascinating insights about this compound:
- Stereochemistry: This compound exhibits a complex stereochemical arrangement that can significantly influence its reactivity and biological activity. The designation of R and S configurations at specific carbon atoms helps in determining the compound's properties.
- Functional Groups: With multiple hydroxyl groups (-OH), it demonstrates the characteristics of polyols. This makes it potentially interesting for various applications in biochemistry, especially in the context of carbohydrate chemistry.
- Natural Occurrence: Compounds with similar structural frameworks are often found in nature, frequently linked to sugars and polysaccharides. The relationship between synthetic derivatives and their natural counterparts can provide valuable insights into metabolic pathways.
- Potential Applications: Due to its polyol nature, this compound may show promise in fields such as pharmaceuticals, food chemistry, and cosmetics, where sugar alcohols are often utilized for their sweetness and humectant properties.
- Research Potential: With ongoing research into stereoisomers and their unique properties, compounds like (3R,4R,5R,6S)-6-methyltetrahydropyran-2,3,4,5-tetrol could potentially lead to the discovery of new drugs or other valuable materials, as scientists continue to explore their diverse functionalities.
In summary, the study of (3R,4R,5R,6S)-6-methyltetrahydropyran-2,3,4,5-tetrol not only highlights the intricacies of its molecular architecture but also opens the door to a multitude of possibilities in various scientific domains. As researchers delve deeper into its properties, exciting discoveries await that could greatly benefit fields ranging from medicinal chemistry to materials science.
Synonyms
L-Rhamnopyranose
6-Deoxy-L-mannopyranose
L-(+)-RHAMNOSE
6-deoxy-Mannose
Mannose, 6-deoxy-
73-34-7
L-Mannopyranose, 6-deoxy-
isodulcit
6-Deoxy-Mannopyranose
CHEBI:62346
6-deoxy-mannopyranoside
6-Deoxy-L-Mannopyranoside
10485-94-6
DTXSID801019197
Rha
ramnose
L-rhamnoses
NSC-287050
DTXCID5022647
CHEBI:26546
CHEBI:62345
DTXCID501477194
222-793-4
(3r,4r,5r,6s)-6-methyltetrahydro-2h-pyran-2,3,4,5-tetraol
3615-41-6 73-34-7
6-Deoxy-L-Mannose
dtxsid7042647
einecs 222-793-4
isodulcitol
l-mannomethylose
L-Rha
L-Rhamnose
locaose
mannomethylose, l-
nsc 2056
nsc 287050
Rha (SNFG)
rhaminopyranose, l-
Rhamnose
rhamnose (mart.)
SNFG:Rha
unii-qn34xc755a
(3R,4R,5R,6S)-6-methyloxane-2,3,4,5-tetrol
Rhamnopyranose
Deoxymannose
DL-Rhamnose
6-Deoxy-DL-mannose
6-deoxy-l(+)-mannose
DL-Mannose, 6-deoxy-
Epitope ID:225177
l-rhamnose for biochemistry
Uridine diphosphate rhamnose
L-(+)-Rhamnose 1-hydrate
SCHEMBL713153
CHEMBL5308434
AKOS017343737
P-(6-deoxy-b-L-mannopyranosyl) ester
Mono(6-deoxy-b-L-mannopyranosyl) ester
BS-10029
P-(6-deoxy-beta-L-mannopyranosyl) ester
Mono(6-deoxy-beta-L-mannopyranosyl) ester
C00507
EN300-1697438
L-(+)-Rhamnose Hydrate = 6-Deoxy-L-mannose Monohydrate
Solubility of (3R,4R,5R,6S)-6-methyltetrahydropyran-2,3,4,5-tetrol
The solubility of the compound (3R,4R,5R,6S)-6-methyltetrahydropyran-2,3,4,5-tetrol, with the chemical formula C6H12O5, can be analyzed based on its structural features.
The solubility can be described succinctly as: highly soluble in water owing to its multiple hydrophilic -OH groups, yet poorly soluble in non-polar solvents.
In summary, the unique structural characteristics of (3R,4R,5R,6S)-6-methyltetrahydropyran-2,3,4,5-tetrol significantly influence its solubility profile, making it an intriguing compound for studies involving solubility behavior.