Interesting facts
Interesting Facts About (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal
(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal is a fascinating compound primarily due to its structural complexity and its significance in various biochemical processes.
Key Highlights:
- Stereochemistry: This compound features four chiral centers, making it a tetrahydroxy derivative. The specific stereochemistry contributes to its unique properties and behaviors in biochemical reactions.
- Natural Occurrence: It plays a role in the metabolism of sugars, being a part of interconversions between different forms of carbohydrates, which are crucial for energy production in living organisms.
- Biochemical Pathways: This compound is involved in several important biochemical pathways, including the synthesis of polysaccharides and glycoproteins, highlighting its role in maintaining cellular functions.
- Potential Applications: Due to its hydroxyl groups, it has potential applications in the pharmaceutical and food industries, where it may serve as a sweetener or a precursor for complex organic syntheses.
- Research Interest: Chemists are particularly interested in studying its reactivity and interactions with other biomolecules, which could lead to new therapeutic approaches in medicine.
The unique combination of stereocenters and functional groups in (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal indeed makes it a subject of study among chemists, as they seek to uncover even more about its properties and potential uses.
Synonyms
3615-41-6
(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal
aldehydo-L-rhamnose
Rhamnose, L-
FEMA No. 3730
QN34XC755A
CHEBI:16055
alpha-L-Rhamnoside
Rhamnose (VAN)
118214-04-3
RNS
NSC-2056
(L)-rhamnose
6-deoxy L-mannose
RHAMNOSE [MI]
Epitope ID:141798
L-RHAMNOSE [FHFI]
RHAMNOSE [WHO-DD]
SCHEMBL25050
HY-N1420
97% (contains <9-12%H2O)
MFCD00136036
AKOS006281392
AKOS015840145
CS-W019751
DB02961
DS-15421
R0013
EN300-343244
Q414109
C01773FD-F731-4717-A3A9-F9DEC1D61326
Solubility of (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal
(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal is a compound with multiple hydroxyl (–OH) groups, which significantly influences its solubility characteristics. As a result of these functional groups, the compound exhibits high polarity, making it more soluble in polar solvents.
Key points regarding its solubility include:
In summary, the extensive hydrogen bonding potential resulting from the numerous hydroxyl groups makes (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal highly soluble in polar environments while limiting its solubility in non-polar mediums.