CAS 202979-51-9
:3,4-Piperidinediol,5-(hydroxymethyl)-, (3R,4R,5S)-
Description:
3,4-Piperidinediol, 5-(hydroxymethyl)-, (3R,4R,5S)- is a chiral organic compound characterized by a piperidine ring with hydroxyl groups at the 3 and 4 positions and a hydroxymethyl group at the 5 position. This compound features a specific stereochemistry, denoted by the (3R,4R,5S) configuration, which influences its biological activity and interactions. The presence of multiple hydroxyl groups contributes to its hydrophilicity, making it soluble in polar solvents. This compound may be of interest in pharmaceutical research due to its potential applications in drug development, particularly in the synthesis of biologically active molecules. Its structural features suggest that it could participate in hydrogen bonding, which may enhance its reactivity and interactions with biological targets. Additionally, the piperidine moiety is often associated with various pharmacological properties, making this compound a candidate for further investigation in medicinal chemistry. As with any chemical substance, safety and handling precautions should be observed, particularly in laboratory settings.
Formula:C6H13NO3
Synonyms:- 3,4-Piperidinediol,5-(hydroxymethyl)-, [3R-(3a,4b,5b)]-
- 5-epi-Isofagomine
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Found 3 products.
3,4-Piperidinediol, 5-(hydroxymethyl)-, (3R,4R,5S)-
CAS:Formula:C6H13NO3Color and Shape:SolidMolecular weight:147.17235-epi-isofagomine
CAS:<p>5-Epi-isofagomine is a piperidine compound that can be used as a synthon for various carbohydrate derivatives. It has been shown to inhibit glycosidases and may be applied in the synthesis of carbohydrates. This compound is synthesized by a stepwise nitro reduction of d-mannitol, followed by an enolate reaction with an appropriate acid chloride. The 5-epi-isofagomine skeleton is obtained by stereoselective polyhydroxylation of the corresponding 2,5-dihydroxybenzaldehyde.</p>Formula:C6H13NO3Purity:Min. 95%Molecular weight:147.17 g/molL-Afegostat
CAS:<p>L-Afegostat (5-epi-Isofagomine), an iminosugar, inhibits glycosidase and β-Glucosidase (K i 30 μM), aids in carbohydrate synthesis.</p>Formula:C6H13NO3Color and Shape:SolidMolecular weight:147.17


