197440-94-1

Basic information

• Product Name: Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{3-hydroxy-5-[(Z)-2-(4-methoxy-phenyl)-vinyl]-phenoxy}-tetrahydro-pyran-3-yl ester
• Synonyms: Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{3-hydroxy-5-[(Z)-2-(4-methoxy-phenyl)-vinyl]-phenoxy}-tetrahydro-pyran-3-yl ester
• CAS NO: 197440-94-1
• Molecular Weight: 572.566
• Mol File: 197440-94-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{3-hydroxy-5-[(Z)-2-(4-methoxy-phenyl)-vinyl]-phenoxy}-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{3-hydroxy-5-[(Z)-2-(4-methoxy-phenyl)-vinyl]-phenoxy}-tetrahydro-pyran-3-yl ester(197440-94-1)
• EPA Substance Registry System: Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{3-hydroxy-5-[(Z)-2-(4-methoxy-phenyl)-vinyl]-phenoxy}-tetrahydro-pyran-3-yl ester(197440-94-1)

Safety Data

• Hazardous Substances Data: 197440-94-1(Hazardous Substances Data)

Upstream product

• 21960-26-9 (4-methoxybenzylidene)triphenylphosphorane 
• 192710-89-7 cis-5-(4-methoxystyryl)benzene-1,3-diol 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 

Downstream Products

• 148766-36-3 cis-piceid 
• 27208-80-6 polydatin 
• 94425-94-2 cis-3,5-dihydroxy-4'-methoxystilbene 3-O-β-D-glucopyranoside 

Relevant articles and documents

Isolation, synthesis, and antiplatelet aggregation activity of resveratrol 3-O-β-D-glucopyranoside and related compounds

Resveratrol 3-O-β-D-glucopyranoside (1) has been isolated from the seeds of Erythrophleum lasianthum (Caesalpinioidae, Leguminosae), a South African plant used in traditional medicine, and has shown antiplatelet aggregation activity. The synthesis of 1, related hydroxystilbenes, and their glucosides has been undertaken to provide larger quantities, for further biological evaluation, and has been accomplished via Wittig reactions followed by glucosylation under phase transfer catalysis.