94356-30-6

Basic information

• Product Name: cis-3,3',5-trihydroxy-4'-methoxystilbene 3-O-β-D-glucopyranoside
• CAS NO: 94356-30-6
• Molecular Weight: 420.416
• Mol File: 94356-30-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: cis-3,3',5-trihydroxy-4'-methoxystilbene 3-O-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: cis-3,3',5-trihydroxy-4'-methoxystilbene 3-O-β-D-glucopyranoside(94356-30-6)
• EPA Substance Registry System: cis-3,3',5-trihydroxy-4'-methoxystilbene 3-O-β-D-glucopyranoside(94356-30-6)

Safety Data

• Hazardous Substances Data: 94356-30-6(Hazardous Substances Data)

Upstream product

• 94356-23-7 rhaponticin 6-gallate 
• 94356-24-8 rhaponticin 2-gallate 
• 94356-25-9 rhaponticin 2''-O-p-coumarate 
• 155-58-8 rhaponticin 
• 621-58-9 3-hydroxy-4-methoxystyrene 
• 709030-16-0 (3-hydroxy-5-iodophenyl) 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 604-68-2 α-D-glucopyranose peracetylate 
• 10272-07-8 3.5-dimethoxyaniline 
• 25245-27-6 1-iodo-3,5-dimethoxybenzene 
• 621-59-0 isovanillin 
• 124530-57-0 Rhaponticin 6''-O-(E)-p-coumarate 

Downstream Products

• 1403836-09-8 rhaponticin 
• 1093135-92-2 C₄₇H₆₇NO₂₉ 
• 266997-55-1 (2S,3R,4S,5R,6R)-2-{3-[(E)-2-(3,4-Dimethoxy-phenyl)-vinyl]-5-methoxy-phenoxy}-3,4,5-trimethoxy-6-methoxymethyl-tetrahydro-pyran 
• 500-65-2 rhapontigenin 
• 113042-92-5 Acetic acid (2R,3S,4R,5S,6S)-3,5-diacetoxy-2-{3-acetoxy-5-[(E)-2-(3-acetoxy-4-methoxy-phenyl)-vinyl]-phenoxy}-6-acetoxymethyl-tetrahydro-pyran-4-yl ester 
• 113042-92-5 (E)-3,3'-diacetoxy-4'-methoxy-5-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)stilbene 

Relevant articles and documents

A short synthesis of rhaponticin and its 3''-fluoroanalog via a wittig/heck-mizoroki route

Rhaponticin and its 3''-fluoroanalog have been prepared from easily accessible starting materials. The key step of these syntheses is the silver carbonate-mediated glycosidation reaction employed for the selective formation of a β -glycosidic bond. A palladium acetate-catalyzed Heck-Mizoroki reaction in triethanolamine established an (E) configuration in the stilbene with simultaneous deprotection of the carbohydrate.

New acylated rhaponticin isolated from Eucalyptus rubida as a repellent against the blue mussel Mytilus edulis

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