Sucrose
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- Molecular formula
- C12H22O11
- CAS Number
- 57-50-1
- IUPAC Name
- (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)tetrahydropyran-3-yl]oxy-tetrahydropyran-3,4,5-triol
- Molecular Weight
- 342.30g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5870g/cm3
- Synonyms
- maltose
Identification
Interesting facts
Interesting Facts about (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)tetrahydropyran-3-yl]oxy-tetrahydropyran-3,4,5-triol
This fascinating compound, often explored in the realm of carbohydrate chemistry, shares characteristics with naturally occurring sugars. Below are some intriguing aspects that highlight its significance:
- Structural Complexity: This compound showcases a complex stereochemistry with multiple chiral centers, which plays a crucial role in its biological activity and functionality.
- Hydroxymethyl Groups: The presence of hydroxymethyl groups contributes to its reactivity and interactions with various biological molecules, including enzymes and receptors.
- Importance in Glycobiology: As part of glycan structures, this compound can influence cell signaling and recognition processes, making it vital for biological research.
- Potential Applications: Its derivatives may have applications in drug development and can serve as important intermediates in the synthesis of more complex molecules.
- Study of Stereochemistry: The diverse configurations of its stereocenters provide an excellent platform for studying stereochemical effects in reactions and interactions.
To quote Sir Isaac Newton, “If I have seen further, it is by standing on the shoulders of giants.” This compound exemplifies how innovative chemical structures contribute to advancements in various fields such as medicinal chemistry, biochemistry, and pharmaceuticals.
Through a better understanding of compounds like this, scientists can pave the way for new discoveries and applications.