4-Phenyl-3-buten-2-one

≥99.5%

Reagent Code: #224708
label
Alias benzyl acetone; benzyl methylene acetone, benzyl acetone, 4-phenyl-3-butene-2-one
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CAS Number 122-57-6

science Other reagents with same CAS 122-57-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.19 g/mol
Formula C₁₀H₁₀O
badge Registry Numbers
EC Number 204-555-1
MDL Number MFCD00008779
thermostat Physical Properties
Melting Point 39-42 °C(lit.)
Boiling Point 260-262 °C(lit.)
inventory_2 Storage & Handling
Density 1.038
Storage Room temperature, avoid light

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of fragrances and flavoring agents due to its aromatic and reactive properties. It serves as a building block in the synthesis of more complex molecules, including pharmaceuticals and fine chemicals. Its α,β-unsaturated ketone structure makes it suitable for Michael addition reactions, enabling the formation of carbon-carbon bonds in synthetic pathways. Also employed in research settings for developing novel compounds with potential biological activity.

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Test Parameter Specification
Purity (%) >=99.5%
Appearance White or light yellow solid or liquid
Infrared Spectrum Conforms to structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿370.00
inventory 100g
10-20 days ฿880.00
inventory 1kg
10-20 days ฿3,900.00
inventory 5kg
10-20 days ฿13,980.00

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4-Phenyl-3-buten-2-one
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Used as an intermediate in organic synthesis, particularly in the production of fragrances and flavoring agents due to its aromatic and reactive properties. It serves as a building block in the synthesis of more complex molecules, including pharmaceuticals and fine chemicals. Its α,β-unsaturated ketone structure makes it suitable for Michael addition reactions, enabling the formation of carbon-carbon bonds in synthetic pathways. Also employed in research settings for developing novel compounds with poten

Used as an intermediate in organic synthesis, particularly in the production of fragrances and flavoring agents due to its aromatic and reactive properties. It serves as a building block in the synthesis of more complex molecules, including pharmaceuticals and fine chemicals. Its α,β-unsaturated ketone structure makes it suitable for Michael addition reactions, enabling the formation of carbon-carbon bonds in synthetic pathways. Also employed in research settings for developing novel compounds with potential biological activity.

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