4-(4-Acetoxyphenyl)-2-butanone

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Reagent Code: #135592
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CAS Number 3572-06-3

science Other reagents with same CAS 3572-06-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.24 g/mol
Formula C₁₂H₁₄O₃
badge Registry Numbers
MDL Number MFCD00008704
thermostat Physical Properties
Boiling Point 123-124°C 0.2mm Hg (Lit.)
inventory_2 Storage & Handling
Density 1.0990g/ml
Storage Room temperature

description Product Description

4-(4-Acetoxyphenyl)-2-butanone is primarily employed as a protected intermediate in organic synthesis for the production of pharmaceuticals, fine chemicals, and fragrances, notably in the preparation of raspberry ketone (4-(4-hydroxyphenyl)-2-butanone). The acetoxy group acts as a removable protecting group for the phenolic hydroxyl, facilitating selective modifications. Its ketone moiety enables versatile reactions for building complex molecular structures. In fragrance applications, it imparts sweet, fruity notes reminiscent of raspberry. Additionally, it supports research in novel synthetic routes and reaction mechanism studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿180.00
inventory 25g
10-20 days ฿380.00
inventory 100g
10-20 days ฿1,120.00
inventory 500g
10-20 days ฿4,720.00
inventory 2.5kg
10-20 days ฿22,290.00

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4-(4-Acetoxyphenyl)-2-butanone
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4-(4-Acetoxyphenyl)-2-butanone is primarily employed as a protected intermediate in organic synthesis for the production of pharmaceuticals, fine chemicals, and fragrances, notably in the preparation of raspberry ketone (4-(4-hydroxyphenyl)-2-butanone). The acetoxy group acts as a removable protecting group for the phenolic hydroxyl, facilitating selective modifications. Its ketone moiety enables versatile reactions for building complex molecular structures. In fragrance applications, it imparts sweet, f

4-(4-Acetoxyphenyl)-2-butanone is primarily employed as a protected intermediate in organic synthesis for the production of pharmaceuticals, fine chemicals, and fragrances, notably in the preparation of raspberry ketone (4-(4-hydroxyphenyl)-2-butanone). The acetoxy group acts as a removable protecting group for the phenolic hydroxyl, facilitating selective modifications. Its ketone moiety enables versatile reactions for building complex molecular structures. In fragrance applications, it imparts sweet, fruity notes reminiscent of raspberry. Additionally, it supports research in novel synthetic routes and reaction mechanism studies.

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