Compound Q&A
How is (1beta,3beta,25R)-3-Hydroxyspirost-5-en-1-yl 6-deoxy-alpha-L-mannopyranosyl-(1->2)-[beta-D-xylopyranosyl-(1->3)]-6-deoxy-beta-D-galactopyranoside (CAS: 41753-55-3) typically synthesized?
Answer
![(1beta,3beta,25R)-3-Hydroxyspirost-5-en-1-yl 6-deoxy-alpha-L-mannopyranosyl-(1->2)-[beta-D-xylopyranosyl-(1->3)]-6-deoxy-beta-D-galactopyranoside](https://static.chemtradehub.com/structs/417/41753-55-3-ebde.webp "(1beta,3beta,25R)-3-Hydroxyspirost-5-en-1-yl 6-deoxy-alpha-L-mannopyranosyl-(1->2)-[beta-D-xylopyranosyl-(1->3)]-6-deoxy-beta-D-galactopyranoside")
This compound is typically synthesized via a multi-step process involving condensation reactions, sugar modifications, and spirocyclic formation. Common catalysts include various transition metals and organocatalysts. The reaction conditions are optimized for high yield and selectivity, often requiring careful control of temperature and pH.
About
CAS No
41753-55-3
English Name
(1beta,3beta,25R)-3-Hydroxyspirost-5-en-1-yl 6-deoxy-alpha-L-mannopyranosyl-(1->2)-[beta-D-xylopyranosyl-(1->3)]-6-deoxy-beta-D-galactopyranoside
Molecular Formula
C44H70O16
Molecular Weight
855.03 g/mol
SMILES
C[C@@H]1CC[C@@]2([C@H]([C@H]3[C@@H](O2)C[C@@H]4[C@@]3(CC[C@H]5[C@H]4CC=C6[C@@]5([C@@H](C[C@@H](C6)O)O[C@H]7[C@@H]([C@H]([C@H]([C@H](O7)C)O)O[C@H]8[C@@H]([C@H]([C@@H](CO8)O)O)O)O[C@H]9[C@@H]([C@@H]([C@H]([C@@H](O9)C)O)O)O)C)C)C)OC1
InChIKey
FHKHGNFKBPFJCB-LYLKFOBISA-N
Last Updated: 2025-10-10 13:51
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