97747-56-3

Basic information

• Product Name: cis-verbascoside
• Synonyms: cis-verbascoside
• CAS NO: 97747-56-3
• Molecular Weight: 624.596
• Mol File: 97747-56-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: cis-verbascoside(CAS DataBase Reference)
• NIST Chemistry Reference: cis-verbascoside(97747-56-3)
• EPA Substance Registry System: cis-verbascoside(97747-56-3)

Safety Data

• Hazardous Substances Data: 97747-56-3(Hazardous Substances Data)

Upstream product

• 61276-17-3 Acteoside 
• 253790-75-9 3,4-di(benzyloxy)phenethyl 2,6-di-O-acetyl-3-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-4-O-(3,4-di-O-benzylcaffeoyl)-β-D-glucopyranoside 
• 253790-73-7 3,4-di(benzyloxy)phenethyl 2,6-di-O-acetyl-3-O-allyl-4-O-(3,4-di-O-benzylcaffeoyl)-β-D-glucopyranoside 
• 253790-74-8 3,4-di(benzyloxy)phenethyl 2,6-di-O-acetyl-4-O-(3,4-di-O-benzylcaffeoyl)-β-D-glucopyranoside 
• 253790-71-5 3,4-di(benzyloxy)phenethyl 2,4-di-O-acetyl-3-O-allyl-6-O-trityl-β-D-glucopyranoside 
• 253790-70-4 3,4-di(benzyloxy)phenethyl 3-O-allyl-6-O-trityl-β-D-glucopyranoside 
• 253790-68-0 3,4-di(benzyloxy)phenethyl 2,4,6-tri-O-acetyl-3-O-allyl-β-D-glucopyranoside 
• 253790-72-6 3,4-di(benzyloxy)phenethyl 2,6-di-O-acetyl-3-O-allyl-β-D-glucopyranoside 
• 253790-69-1 3,4-di(benzyloxy)phenethyl 3-O-allyl-β-D-glucopyranoside 
• 253790-67-9 2,4,6-tri-O-acetyl-3-O-allyl-α-D-glucopyranosyl chloride 
• 39698-00-5 acetyl 2,4,6-tri-O-acetyl-3-O-allyl-β-D-glucopyranoside 
• 54429-62-8 (E)-3-(3,4-bis(benzyloxy)phenyl)acrylic acid 
• 96826-11-8 2-<3,4-bis(benzyloxy)phenyl>ethanol 
• 253790-76-0 3,4-di(benzyloxy)phenethyl 3-O-(α-L-rhamnopyranosyl)-4-O-(3,4-di-O-benzylcaffeoyl)-β-D-glucopyranoside 

Downstream Products

• 86495-62-7 per-O-acetyl-verbascoside 
• 10597-60-1 hydroxytyrosol 
• 3843-74-1 Methyl caffeate 
• 64142-09-2 acteoside tetramethyl ether 
• 2280-44-6 D-Glucose 
• 73-34-7 L-rhamnose 
• 86495-62-7 acetate of 3,4-dihydroxy-β-phenethyl-O-α-L-rhamnopyranosyl-(1<*>3)-4-O-caffeoyl-β-D-glucopyranoside 
• 331-39-5 caffeic acid 
• 3615-41-6 L-Rhamnose 
• 50-99-7 D-glucose 

Relevant articles and documents

NINE PHENETHYL ALCOHOL GLYCOSIDES FROM STACHYS SIEBOLDII

Three new phenethyl alcohol glycosides together with six known compounds have been isolated from the leaves of Stachys sieboldii.On the basis of chemical and spectral analyses, the structures of three new compounds named stachysosides A, B and C have been established as 2-(3,4-dihydroxyphenyl)ethyl O-α-L-arabinopyranosyl-(1->2)-α-L-rhamnopyranosyl-(1->3)-4-O-E-caffeoyl-β-D-glucopyranoside, 2-(3,4-dihydroxyphenyl)ethyl O-α-L-arabinopyranosyl-(1->2)-α-L-rhamnopyranosyl-(1->3)-4-O-E-feruloyl-β-D-glucopyranoside and 2-(3-hydroxy-4-methoxyphenyl)ethyl O-α-L-arabinopranosyl-(1->2)-α-L-rhamnopyranosyl-(1->3)-4-O-E-feruloyl-β-D-glucopyranoside, respectively.

An Approach to the Synthesis of Electron-Rich and Hindered Esters and Its Application to the Synthesis of Acteoside

Electron-rich esters are ubiquitously distributed in natural products and play a central role in bioactivities. Herein, we disclose an efficient, mild, and general esterification approach to the synthesis of these esters by employing gold(I)-catalyzed acylation reaction with alkyne-tethered mixed anhydrides and alcohols. This method can be applied to ester-bond formation in complex substrates and facilitates efficient synthesis of acteoside, which belongs to the family of phenylethanoid glycosides and possesses a broad range of bioactivities.

Total Synthesis of the Phenylpropanoid Glycoside, Acteoside

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