The chemical substance known as b-D-Glucopyranoside with the specific stereochemical configuration (1aS,1bS,2S,5aR,6S,6aS) and CAS number 221014-58-0 is a complex glycoside. It features a glucopyranoside moiety, which is a six-membered cyclic form of glucose, linked to a unique hexahydro-oxireno-cyclopenta-pyran structure. This compound exhibits characteristics typical of glycosides, including solubility in polar solvents due to the presence of hydroxyl groups. The presence of the phenyl group and the 6-deoxy-2-O-[(2E)-1-oxo-3-phenyl-2-propen-1-yl]-a-L-mannopyranosyl unit suggests potential biological activity, possibly influencing its interaction with biological systems. The stereochemistry indicated by the specific configuration of the chiral centers may affect its reactivity and biological properties, including enzyme interactions and binding affinities. Overall, this compound's structural complexity and functional groups suggest it may have applications in medicinal chemistry or as a biochemical probe.

b-D-Glucopyranoside,(1aS,1bS,2S,5aR,6S,6aS)-6-[[6-deoxy-2-O-[(2E)-1-oxo-3-phenyl-2-propen-1-yl]-a-L-mannopyranosyl]oxy]-1a,1b,2,5a,6,6a-hexahydro-1a-(hydroxymethyl)oxireno[4,5]cyclopenta[1,2-c]pyran-2-yl

221014-58-0: The chemical substance known as b-D-Glucopyranoside with the specific stereochemical configuration (1aS,1bS,2S,5aR,6S,6aS) and CAS number 221014-58-0 is a complex glycoside. It features a glucopyranoside moiety, which is a six-membered cyclic form of glucose, linked to a unique hexahydro-oxireno-cyclopenta-pyran structure. This compound exhibits characteristics typical of glycosides, including solubility in polar solvents due to the presence of hydroxyl groups. The presence of the phenyl group and the 6-deoxy-2-O-[(2E)-1-oxo-3-phenyl-2-propen-1-yl]-a-L-mannopyranosyl unit suggests potential biological activity, possibly influencing its interaction with biological systems. The stereochemistry indicated by the specific configuration of the chiral centers may affect its reactivity and biological properties, including enzyme interactions and binding affinities. Overall, this compound's structural complexity and functional groups suggest it may have applications in medicinal chemistry or as a biochemical probe.

<p>Verbaspinoside is a useful organic compound for research related to life sciences. The catalog number is T125312 and the CAS number is 221014-58-0.</p>

CAS 221014-58-0

b-D-Glucopyranoside,(1aS,1bS,2S,5aR,6S,6aS)-6-[[6-deoxy-2-O-[(2E)-1-oxo-3-phenyl-2-propen-1-yl]-a-L-mannopyranosyl]oxy]-1a,1b,2,5a,6,6a-hexahydro-1a-(hydroxymethyl)oxireno[4,5]cyclopenta[1,2-c]pyran-2-yl

Verbaspinoside

Ref: TM-T125312