143572-86-5

Usage

Potential pharmacological properties

+ Antibacterial
+ Antiviral
+ Antifungal
Potential use in food and cosmetic industry due to pleasant scent and flavor

Potential therapeutic effects on various health conditions

+ Antioxidant
+ Anti-inflammatory

Upstream product

• 1268603-53-7 methyl 2-(3-(benzyloxy)-2-oxopropyl)-4,6-dimethoxybenzoate 
• 6110-37-8 methyl 2,4-dimethoxy-6-methylbenzoate 
• 104863-68-5 2-(benzyloxy)-N-methoxy-N-methylacetamide 
• 1350450-12-2 C₁₃H₁₄O₅ 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 846003-80-3 6,8-dimethoxy-3-hydroxymethylisocoumarin 

Downstream Products

• 1269609-35-9 6-(2-(2-((benzyloxy)methyl)-4-hydroxy-5,7-dimethoxynaphthalen-3-yl)-4,6-dimethoxyphenyl)-2-methyl-2H-pyran-4(3H)-one 
• 1268603-56-0 11-((benzyloxy)methyl)-2,4,7,9-tetramethoxy-6H-dibenzo[c,h]chromen-6-one 
• 1268603-57-1 (1Z,4E)-1-(2-(3-((benzyloxy)methyl)-1-hydroxy-6,8-dimethoxynaphthalen-2-yl)-4,6-dimethoxyphenyl)-1-hydroxyhexa-1,4-dien-3-one 
• 1268603-55-9 2-(3-((benzyloxy)methyl)-1-hydroxy-6,8-dimethoxynaphthalen-2-yl)-4,6-dimethoxybenzoic acid 
• 1268603-54-8 C₃₀H₃₂O₉ 

Relevant academic research and scientific papers

Total synthesis of (±)-cephalosol

A concise and efficient total synthesis of (±)-cephalosol has been completed (5 steps from known ester 5, 39% overall yield), featuring a Cu(II)-promoted haloisocoumarin formation and sequential Suzuki cross-coupling/intramolecular oxo-Michael addition.

Synthetic studies toward A-74528

A potentially biomimetic approach toward the complex polyketide A-74528 is described. It is based on highly substituted biaryl compounds, synthesized using advanced cross-coupling and condensation methodologies.