6342-75-2

Usage

Uses

Used in Food Industry:
1-(2-methoxy-3-methylphenyl)ethanone is used as a flavoring agent for imparting sweet and floral notes to various food products.
Used in Cosmetic Industry:
1-(2-methoxy-3-methylphenyl)ethanone is used as a fragrance ingredient to add pleasant scents to cosmetic products.
Used in Pharmaceutical Industry:
1-(2-methoxy-3-methylphenyl)ethanone is used as a chemical intermediate in the synthesis of pharmaceuticals.
Used in Personal Care Products:
1-(2-methoxy-3-methylphenyl)ethanone is used as an antimicrobial and antioxidant agent in various personal care products to enhance their shelf life and provide additional benefits to the users.
It is important to handle and store 1-(2-methoxy-3-methylphenyl)ethanone according to safety guidelines to prevent potential health hazards.

Upstream product

• 77-78-1 dimethyl sulfate 
• 74-88-4 methyl iodide 
• 7647-01-0 hydrogenchloride 
• 103095-90-5 1-(2-methoxy-3-methyl-phenyl)-ethanone oxime 
• 876-02-8 4-hydroxy-3-methylphenyl methyl ketone 
• 584-08-7 potassium carbonate 
• 699-91-2 2-acetyl-6-methylphenol 
• 83-40-9 3-methylsalicylic acid 

Downstream Products

• 103095-90-5 1-(2-methoxy-3-methyl-phenyl)-ethanone oxime 
• 859330-53-3 2-methoxy-1-methyl-3-(prop-1-en-2-yl)benzene 

Relevant academic research and scientific papers

Iridium-Catalyzed C(sp3)?H Addition of Methyl Ethers across Intramolecular Carbon–Carbon Double Bonds Giving 2,3-Dihydrobenzofurans

Intramolecular addition of an O-methyl C(sp3)?H bond across a carbon-carbon double bond occurs in the iridium-catalyzed reaction of methyl 2-(propen-2-yl)phenyl ethers. The Ir/(S)-DTBM-SEGPHOS catalyst promotes the reaction efficiently in toluene at 110–135 °C to afford 3,3-dimethyl-2,3-dihydrobenzofurans. Enantioselective C(sp3)?H addition is achieved in the reaction of methyl 2-(1-siloxyethenyl)phenyl ethers, affording enantioenriched 3-hydroxy-2,3-dihydrobenzofuran derivatives with up to 96% ee. (Figure presented.).

Concise total synthesis of (±)-dasyscyphin D

The first and efficient total synthesis of (±)-dasyscyphin D was achieved in 9 steps with 22.6% overall yield. The key steps involved a PtCl 2-catalyzed pentannulation reaction and acid-catalyzed double Robinson annulations.

Calcium receptor-active molecules

The present invention relates to the different roles inorganic ion receptors have in cellular and body processes. The present invention features: (1) molecules which can modulate one or more inorganic ion receptor activities, preferably the molecule can m