203179-62-8

Basic information

• Product Name: 3,5-dimethoxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)-trans-cinnamaldehyde
• Synonyms: 3,5-dimethoxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)-trans-cinnamaldehyde
• CAS NO: 203179-62-8
• Molecular Weight: 538.505
• Mol File: 203179-62-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3,5-dimethoxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)-trans-cinnamaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dimethoxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)-trans-cinnamaldehyde(203179-62-8)
• EPA Substance Registry System: 3,5-dimethoxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)-trans-cinnamaldehyde(203179-62-8)

Safety Data

• Hazardous Substances Data: 203179-62-8(Hazardous Substances Data)

Upstream product

• 4206-58-0 (E)-sinapinaldehyde 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 83-87-4 D-glucose pentaacetate 
• 117685-21-9 3,5-dimethoxy-4-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyloxy)benzaldehyde 
• 71686-40-3 (E)-2,6-dimethoxy-4-(3-oxoprop-1-en-1-yl)phenyl acetate 
• 53669-33-3 4-acetoxy-3,5-dimethoxybenzaldehyde 
• 134-96-3 syringic aldehyde 

Downstream Products

• 118-34-3 syringin 
• 154461-65-1 sinapyl aldehyde 4-O-β-D-glucopyranoside 
• 20675-96-1 Syringenin 
• 203179-64-0 (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(4-((E)-3-hydroxyprop-1-en-1 -yl)-2,6-dimethoxyphenoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate 

Relevant articles and documents

Total Syntheses and Anti-inflammatory Activities of Syringin and Its Natural Analogues

Syringin (1), a natural bioactive glucoside isolated from the root of Acanthopanax senticosus (Rupr. Maxim.) Harms, possesses significant anti-inflammatory activity. In this study, we have accomplished the total syntheses of syringin (1), along with its natural analogues 2-12, from a common starting material, syringaldehyde (13), in 4-8 steps with an overall yields of 11.8-61.3%. The anti-inflammatory activities of these compounds were determined against NO production in the LPS-stimulated RAW264.7 cells. Among them, compounds 1-5, 7, and 9 exhibited different levels of anti-inflammatory activity.