7228-35-5

Usage

Uses

Used in Food Industry:
Sesamol methyl ether is used as a food preservative for its antioxidant properties, which help to extend the shelf life of food products and maintain their quality.
Used in Pharmaceutical Industry:
Sesamol methyl ether is used as a protective agent for cells against oxidative damage and inflammation, which may contribute to the development of health-promoting pharmaceutical products.
Used in Cosmetics Industry:
Sesamol methyl ether is used in skin care products for its ability to protect the skin from UV damage and reduce the appearance of wrinkles, making it a valuable ingredient for anti-aging and skin protection formulations.

Upstream product

• 504421-93-6 2,4-diacetoxy-1-iodobenzene 
• 673477-43-5 1-ethynyl-2-methoxy-4,5-methylenedioxybenzene 
• 583-55-1 1-Bromo-2-iodobenzene 

Downstream Products

• 10022-35-2 1-bromo-2-methoxy-4,5-methylenedioxybenzene 
• 5780-00-7 2-methoxy-4,5-methylenedioxybenzaldehyde 
• 77357-51-8 3-methyl-4-methoxy-1,2-dihydroxybenzene 
• 607351-61-1 3-methyl-4-methoxy-1,2-benzoquinone 
• 138958-73-3 1-<2-methoxy-4,5-(methylenedioxy)phenyl>-2-(4-methoxyphenyl)ethane 
• 138958-74-4 1-<2-methoxy-4,5-(methylenedioxy)phenyl>-4-(4-methoxyphenyl)butane 
• 1219118-23-6 1-(2-hydroxy-3-methoxy-5-methylphenyl)-2-methoxybenzodioxole 
• 533-31-3 Sesamol 
• 1148136-30-4 (±)-4-isopropyl-5-methoxy-7,7,10a-trimethyl-8,9,10,10a-tetrahydro-7H-fluoreno[3,4-d][1,3]dioxole 
• 1148136-35-9 (±)-(7-isopropyl-6-methoxybenzo[d][1,3]dioxol-5-yl)(2,6,6-trimethylcyclohex-1-en-1-yl)methanol 

Relevant academic research and scientific papers

The Winding Road towards an Atropo-enantioselective ‘ARYNE Coupling’

For the first time, the challenging atropo-enantioselective coupling of in-situ generated arynes and aryllithiums in the presence of a chiral ligand of lithium was investigated. This preliminary study demonstrates the feasibility of this concept, by affording enantioenriched axially chiral biaryls even in the case of products showing a high degree of steric congestion around the newly created aryl?aryl bond.

Synthesis of cicerfuran, an antifungal benzofuran, and some related analogues

Routes were investigated for the synthesis of cicerfuran, a hydroxylated benzofuran from wild chickpea implicated in resistance to Fusarium wilt, and some of its analogues. A novel method is described for the synthesis of oxygenated benzofurans by epoxidation and cyclisation of 2′-hydroxystilbenes. The stilbene intermediates required could be synthesised by palladium-catalysed coupling of styrenes with mono-oxygenated aryl halides but not with di-oxygenated aryl halides. Stilbenes corresponding to the latter were synthesised by Wittig reactions.