1-(3-Ethoxy-4-methoxyphenyl)ethanone

98%

Reagent Code: #182828
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CAS Number 31526-71-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.23 g/mol
Formula C₁₁H₁₄O₃
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure contains methoxy and ethoxy substituents that can influence electronic and steric properties, making it suitable for use in the development of bioactive molecules. Commonly employed in the synthesis of flavor and fragrance compounds due to the aromatic characteristics imparted by the substituted phenyl ring. Also utilized in the production of agrochemicals and dyes where alkoxy-substituted acetophenone derivatives are required. The ketone functional group allows for further chemical transformations such as reductions, condensations, and nucleophilic additions, enhancing its versatility in synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,230.00
inventory 1g
10-20 days ฿3,070.00
inventory 5g
10-20 days ฿9,560.00
inventory 25g
10-20 days ฿32,210.00
inventory 100g
10-20 days ฿96,650.00
inventory 500g
10-20 days ฿386,600.00
1-(3-Ethoxy-4-methoxyphenyl)ethanone
Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure contains methoxy and ethoxy substituents that can influence electronic and steric properties, making it suitable for use in the development of bioactive molecules. Commonly employed in the synthesis of flavor and fragrance compounds due to the aromatic characteristics imparted by the substituted phenyl ring. Also utilized in the production of agrochemicals and dyes where alkoxy-substituted acetophenone derivatives are required. The ketone functional group allows for further chemical transformations such as reductions, condensations, and nucleophilic additions, enhancing its versatility in synthetic routes.
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