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CAS 65730-00-9

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N-[(2R,4R,5S)-2-allyloxy-4-benzyloxy-5-hydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide

Description:
N-[(2R,4R,5S)-2-allyloxy-4-benzyloxy-5-hydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide, with CAS number 65730-00-9, is a complex organic compound characterized by its unique structural features, including a tetrahydropyran ring and multiple functional groups such as acetamide, hydroxyl, and ether linkages. This compound exhibits chirality due to the presence of multiple stereocenters, which contributes to its potential biological activity. The allyloxy and benzyloxy substituents enhance its lipophilicity, potentially influencing its solubility and permeability in biological systems. The hydroxymethyl group may participate in hydrogen bonding, affecting its interactions with other molecules. Such structural characteristics suggest that this compound could have applications in medicinal chemistry, particularly in the development of pharmaceuticals or as a biochemical probe. However, specific properties such as melting point, boiling point, and solubility would require empirical measurement or detailed literature references for precise characterization.
Formula:C18H25NO6
InChI:InChI=1/C18H25NO6/c1-3-9-23-18-15(19-12(2)21)17(16(22)14(10-20)25-18)24-11-13-7-5-4-6-8-13/h3-8,14-18,20,22H,1,9-11H2,2H3,(H,19,21)/t14?,15?,16-,17-,18-/m1/s1
SMILES:C=CCO[C@H]1C([C@H]([C@@H](C(CO)O1)O)OCc1ccccc1)N=C(C)O
Synonyms:
  • Allyl 2-(Acetylamino)-2-deoxy-3-O-benzyl--D-glucopyranoside
  • 2-Propenyl 2-(Acetylamino)-2-deoxy-3-O-benzyl--D-glucopyranoside
  • Allyl-2-acetamido-3-O-benzyl-2-deoxy-b-D-glucopyranose
  • 2-Propenyl 2-(Acetylamino)-2-deoxy-3-O-(phenylmethyl)--D-glucopyranoside
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