Interesting facts
              Interesting Facts About 6-(Hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol
6-(Hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol is a fascinating organic compound that plays a significant role in various fields, particularly in biochemistry and medicinal chemistry. Here are some intriguing aspects of this compound:
- Biosynthesis: This compound is involved in the metabolism of carbohydrates, serving as an intermediate product. Understanding its role can shed light on metabolic pathways.
- Structure and Function: The bicyclic structure of 6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol allows it to easily participate in both acid-base reactions and complexation with metal ions. This reactivity can be exploited in various synthetic processes.
- Hydroxymethyl Groups: The presence of hydroxymethyl groups enhances its potential for biocompatibility, making it a candidate for applications in drug formulation and design.
- Potential Applications: Researchers are investigating its application in the field of pharmaceuticals due to its unique properties and structural features, which could lead to novel therapeutic agents.
- Natural Occurrence: This compound can be found in some natural products, signaling its importance in ecological and biological systems.
In conclusion, the study of 6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol not only uncovers the intricate details of carbohydrate metabolism but also opens avenues for innovation in medicinal chemistry. As scientific exploration continues, we may discover even more compelling characteristics of this intriguing compound!
Synonyms
          Hexose
          Hexopyranose
          hexopyranoside
          6-(hydroxymethyl)oxane-2,3,4,5-tetrol
          D-[4,6-13C2]glucose
          42752-07-8
          D-Mannose-6-13C
          D-(+)-Mannose
          D-Mannose-2-13C
          b-d-glucose
          D-[1-18O]glucose
          D-Mannose-1-C-d
          D-[2,5-13C2]glucose
          D-[4,5-13C2]glucose
          D-[1-13C]gulose
          D-[2-13C]gulose
          D-[3-13C]galactose
          D-[1-13c,1-2h]glucose
          ALPHA-D-GLUCOSEANHYDROUS
          D-[11-13C]TALOSE
          L-[UL-13C6]galactose
          DTXSID80858960
          NSC8102
          Glucose Oxidase from Aspergillus niger,
          D-[2-2H]galactose
          D-[4-2H]galactose
          .beta.-D-Glucopyranose
          B-D-ALLOPYRANOSE
          D-[2-13C]talose
          D-[3-13C]glucose
          L-[2-13C]glucose
          D-[5-13C]galactose
          D-[6-13C,6,6'-2H2]GLUCOSE
          (3R,4S,5R,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol
          BETA-D-GLUCOSE (CONTAINS ALPHA-D-GLUCOSE)
          D-[1,6-13C2,6,6'-2H2]GLUCOSE
          L-(-)-ALLOSE
          D-[3-2H]GALACTOSE
          D-[1,2-13C2]galactose
          D-[6,6'-2H2]galactose
          D-hexose
          Hexopyranose #
          115973-81-4
          39392-62-6
          478529-30-5
          D-[4,5-2H2]GLUCOSE
          .alpha.-D-Glucose
          D-[4,5,6,6'-2H4]glucose
          Allose, D-
          D(+)-Mannose
          ZYMOSAN
          478518-56-8
          478518-63-7
          478518-66-0
          478518-71-7
          70849-16-0
          D-[4-2H]glucose
          26655-34-5
          .alpha.-D-Glucopyranose
          .alpha.-d-Galactopyranose
          (2S,3R,4S,5R,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol
          D-[3-2H]GLUCOSE
          157171-80-7
          201136-45-0
          288846-86-6
          35669-34-2
          39392-65-9
          478518-62-6
          54724-00-4
          64429-86-3
          70849-25-1
          86595-19-9
          D-[4,5,6-13C3]glucose
          an aldopyranose
          a pyranose
          NSC-8102
          Unknown Hexose
          MFCD00064122
          MFCD00066772
          NSC-144657
          ?-D-Galactose
          Allopyranose, D-
          106032-60-4
          287100-64-5
          40825-89-6
          478518-58-0
          478518-70-6
          478519-05-0
          478529-33-8
          478529-48-5
          478529-49-6
          83379-36-6
          D-glucose anhydrous
          Unknown Hexopyranose
          .alpha.-d-Galactose
          Unknown Hexopyranoside
          alpha-d-(+)-glucose
          GALACTOSE, (D)
          MolMap_000072
          SCHEMBL34307
          SCHEMBL20094856
          SCHEMBL21123450
          SCHEMBL23758905
          CHEBI:18133
          DTXCID10196988
          DTXCID40202844
          CHEBI:167473
          HMS3373C02
          HMS3373E09
          HMS3744K13
          23403-54-5
          478529-47-4
          51517-59-0
          579-36-2
          DAA64673
          DUA51863
          DUA51871
          DUA52930
          JAA01072
          PCA42986
          QEA97381
          VCA84916
          BBL012219
          NSC144657
          NSC274237
          NSC287045
          STL163560
          AKOS000119941
          AKOS016038567
          AKOS022061531
          AKOS037503714
          CCG-272298
          NSC-287045
          SB44851
          SB45285
          SB47940
          Zymosan A from Saccharomyces cerevisiae
          DA-19781
          SY008815
          SY012757
          SY015251
          SY057403
          VS-03240
          6-methyloltetrahydropyran-2,3,4,5-tetrol
          DB-051616
          DB-055683
          DB-112935
          NS00069768
          NS00076953
          EN300-33349
          C00738
          51DB4B86-692B-40EA-A7AD-4B20C8174CBE
          WURCS=2.0/1,1,0/(axxxxh-1x_1-5_2*NCC/3=O)/1/
          175348-09-1
              
Solubility of 6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol (C6H12O6)
The solubility of 6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol, a polyol compound, is generally characterized by its significant ability to dissolve in water. This characteristic is primarily due to the presence of multiple hydroxyl (–OH) groups, which can form hydrogen bonds with water molecules, enhancing its solubility. Here are some key points regarding its solubility:
In conclusion, 6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol is highly soluble in water, making it useful in various applications where aqueous solutions are beneficial. As mentioned, the presence of numerous hydroxyl groups plays a critical role in this property.