4-Phenyl-3-buten-2-one

>98.0%(GC)

Reagent Code: #224707
label
Alias benzyl acetone; benzyl acetone, benzyl acetone, 4-phenyl-3-butene-2-one
fingerprint
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 flavor compounds due to its aromatic and reactive α,β-unsaturated ketone structure. It serves as a building block in the synthesis of more complex molecules, including pharmaceuticals and fine chemicals. Its conjugated system allows for participation in Michael addition reactions, making it valuable in creating carbon-carbon bonds in synthetic pathways. Also employed in research settings for developing novel organic compounds with potential biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿300.00
inventory 500g
10-20 days ฿850.00
inventory 2.5kg
10-20 days ฿3,500.00
inventory 10kg
10-20 days ฿13,500.00

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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 flavor compounds due to its aromatic and reactive α,β-unsaturated ketone structure. It serves as a building block in the synthesis of more complex molecules, including pharmaceuticals and fine chemicals. Its conjugated system allows for participation in Michael addition reactions, making it valuable in creating carbon-carbon bonds in synthetic pathways. Also employed in research settings for developing novel or

Used as an intermediate in organic synthesis, particularly in the production of fragrances and flavor compounds due to its aromatic and reactive α,β-unsaturated ketone structure. It serves as a building block in the synthesis of more complex molecules, including pharmaceuticals and fine chemicals. Its conjugated system allows for participation in Michael addition reactions, making it valuable in creating carbon-carbon bonds in synthetic pathways. Also employed in research settings for developing novel organic compounds with potential biological activity.

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