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D-(+)-Fucose

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Identification
Molecular formula
C6H12O5
CAS number
3615-37-0
IUPAC name
3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol
State
State

At room temperature, D-(+)-Fucose is a solid. It is stable under ordinary conditions and can exist in various crystalline forms.

Melting point (Celsius)
140.00
Melting point (Kelvin)
413.00
Boiling point (Celsius)
548.75
Boiling point (Kelvin)
821.90
General information
Molecular weight
164.16g/mol
Molar mass
164.1600g/mol
Density
1.6940g/cm3
Appearence

D-(+)-Fucose typically appears as a white crystalline solid. It is commonly found in powder form and is known for its sweet taste. Its crystals are often fine and exhibit high solubility in water.

Comment on solubility

Solubility of 3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol (C6H12O5)

The solubility of 3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol is quite noteworthy due to its intricate structure, which incorporates multiple functional groups that can influence its interaction with solvents. Here are some key points regarding its solubility:

  • Polarity: The presence of multiple hydroxyl (–OH) groups enhances the molecule's hydrophilicity, allowing it to readily interact with polar solvents like water.
  • Sugar-like Structure: Considering its sugar-like framework, it is expected to dissolve well in aqueous solutions, similar to other carbohydrate derivatives.
  • Amine Group: The amine functional group adds to the molecule's potential to participate in hydrogen bonding, which further promotes solubility in polar environments.
  • Concentration Dependence: While it is anticipated to have good solubility in water, specific concentrations might influence its saturation point, affecting how much can dissolve.

In summary, 3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol exhibits a strong tendency to be soluble in polar solvents, making it a versatile compound in various applications. Its unique structure, comprising both amino and hydroxymethyl groups, significantly contributes to its solubility properties.

Interesting facts

Interesting Facts about 3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol

3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol is a fascinating compound with several intriguing properties and implications in the field of chemistry and biochemistry. Here are some notable aspects:

  • Structural Features: This compound belongs to a class of molecules known as carbohydrates. Its structure exhibits a tetrahydropyran ring, which is a six-membered ring that contributes to its unique chemical behavior.
  • Biological Relevance: The presence of amino and hydroxymethyl groups suggests potential roles in biological systems, possibly related to amino sugars that are vital for cellular processes.
  • Synthesis Potential: The ability to modify the hydroxymethyl and amino groups may lead to the development of derivatives with enhanced biological activity, making it a subject of interest in drug design and pharmacology.
  • Potential Uses: Compounds like this one can serve as intermediates in synthesizing more complex molecules, which are critical in the production of pharmaceuticals, agrochemicals, and other functional materials.

As one delves deeper into the study of 3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol, it's essential to consider its implications in *medicinal chemistry* and its potential impact on health-related applications. According to a well-known chemist, “The intersection of structural diversity and biological activity is where the magic happens in molecular design.”
This emphasizes the compound's significance as a platform for exploring new therapeutics.

In summary, 3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol is not just a simple compound, but rather a gateway to understanding more complex biochemical interactions and the potential for innovative applications within the scientific community.

Synonyms
2-Amino-2-Deoxy-Hexose
Hexosamine
HexN
3-amino-6-(hydroxymethyl)oxane-2,4,5-triol
a-D-Glucopyranose, 2-amino-2-deoxy-
a-D-Galactopyranose, 2-amino-2-deoxy-
b-D-Galactopyranose, 2-amino-2-deoxy-
579-33-9
686298-83-9
D-2-Galactosamine
2-Amino-2-deoxyhexopyranose
Glucose, 2-amino-2-deoxy-
D-Glucosaminehydrochloride
a hexosamine
D-Mannopyranose, 2-amino-2-deoxy-
Mannopyranose, 2-amoino-2-deoxy-, D-
MANNOPYRANOSE, 2-AMINO-2-DEOXY-
Oprea1_097569
2-Amino-2-Deoxy-Hexopyranose
SCHEMBL1651713
2-Amino-2-Deoxy-Hexopyranoside
CHEBI:24586
DTXSID90859064
CHEBI:180999
MSWZFWKMSRAUBD-UHFFFAOYSA-N
AKOS026749894
A8990
NS00096418
3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol
C9301313-1F98-4F89-90BE-0E4B76394223