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CAS 1240390-32-2

:

(3S,4S)-3-Aminotetrahydro-2H-pyran-4-ol

Description:
(3S,4S)-3-Aminotetrahydro-2H-pyran-4-ol is a chiral organic compound characterized by its tetrahydropyran ring structure, which features an amino group and a hydroxyl group. The presence of these functional groups contributes to its potential as a building block in organic synthesis and pharmaceutical applications. The stereochemistry indicated by the (3S,4S) designation suggests specific spatial arrangements of the substituents around the chiral centers, which can significantly influence the compound's reactivity and biological activity. This compound is typically colorless to pale yellow and may exhibit solubility in polar solvents due to the hydroxyl group. Its molecular interactions can be influenced by hydrogen bonding, making it relevant in various chemical reactions and biological processes. As with many amines and alcohols, it may participate in nucleophilic reactions, and its chirality could be crucial for its interaction with biological targets, potentially leading to enantioselective outcomes in medicinal chemistry.
Formula:C5H11NO2
InChI:InChI=1S/C5H11NO2/c6-4-3-8-2-1-5(4)7/h4-5,7H,1-3,6H2/t4-,5-/m0/s1
InChI key:InChIKey=KUCSFTQJADYIQH-WHFBIAKZSA-N
SMILES:N[C@@H]1[C@@H](O)CCOC1
Synonyms:
  • (3S,4S)-3-Aminotetrahydro-2H-Pyran-4-Ol
  • 2-Amino-1,5-anhydro-2,4-dideoxy-<span class="text-smallcaps">L</span>-threo-pentitol
  • <span class="text-smallcaps">L</span>-threo-Pentitol, 2-amino-1,5-anhydro-2,4-dideoxy-
  • 2-Amino-1,5-anhydro-2,4-dideoxy-L-threo-pentitol
  • L-threo-Pentitol, 2-amino-1,5-anhydro-2,4-dideoxy-
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