6342-75-2

Basic information

• Product Name: 1-(2-methoxy-3-methylphenyl)ethanone
• CAS NO: 6342-75-2
• Molecular Formula: C₁₀H₁₂O₂
• Molecular Weight: 164.2011
• Mol File: 6342-75-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 248.9°C at 760 mmHg
• Flash Point: 101.7°C
• Density: 1.018g/cm³
• Vapor Pressure: 0.0236mmHg at 25°C
• Refractive Index: 1.504
• CAS DataBase Reference: 1-(2-methoxy-3-methylphenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-methoxy-3-methylphenyl)ethanone(6342-75-2)
• EPA Substance Registry System: 1-(2-methoxy-3-methylphenyl)ethanone(6342-75-2)

Safety Data

• Hazardous Substances Data: 6342-75-2(Hazardous Substances Data)

Usage

General Description

1-(2-methoxy-3-methylphenyl)ethanone, also known as 2-Methoxy-3-methylacetophenone, is an organic compound with the chemical formula C10H12O2. It is a pale yellow liquid with a sweet, floral odor. This chemical is commonly used as a fragrance and flavoring agent in the food and cosmetic industries. It is also used in the synthesis of pharmaceuticals and other organic compounds. Additionally, it has antimicrobial and antioxidant properties, making it suitable for use in various personal care products. Despite its various applications, 1-(2-methoxy-3-methylphenyl)ethanone should be handled and stored 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 articles and documents

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.).

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