709030-16-0

Basic information

• Product Name: (3-hydroxy-5-iodophenyl) 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside
• Synonyms: (3-hydroxy-5-iodophenyl) 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside
• CAS NO: 709030-16-0
• Molecular Weight: 566.301
• Mol File: 709030-16-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3-hydroxy-5-iodophenyl) 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: (3-hydroxy-5-iodophenyl) 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside(709030-16-0)
• EPA Substance Registry System: (3-hydroxy-5-iodophenyl) 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside(709030-16-0)

Safety Data

• Hazardous Substances Data: 709030-16-0(Hazardous Substances Data)

Upstream product

• 604-68-2 α-D-glucopyranose peracetylate 
• 10272-07-8 3.5-dimethoxyaniline 
• 25245-27-6 1-iodo-3,5-dimethoxybenzene 
• 64339-43-1 5-iodoresorcinol 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 

Downstream Products

• 155-58-8 rhaponticin 
• 62502-04-9 (E)-1-(3-acetoxy-5-O-2,3,4,6-tetraacetyl-β-D-glucopyranosidophenyl)-2-(4'-acetoxyphenyl)ethene 
• 27208-80-6 polydatin 
• 709030-17-1 3-acetoxy-5-iodophenyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 

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.