1-Phenylbuta-2,3-Dien-1-One

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Reagent Code: #227758
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CAS Number 69626-39-7

science Other reagents with same CAS 69626-39-7

blur_circular Chemical Specifications

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Weight 144.17 g/mol
Formula C₁₀H₈O
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Storage Room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of substituted allenes and heterocyclic compounds. It participates in cycloaddition reactions and metal-catalyzed couplings to build complex molecular frameworks found in bioactive molecules. Commonly employed in the development of pharmaceuticals and agrochemicals due to its reactive α,β-unsaturated ketone functionality and conjugated allene structure. Also utilized in research settings for studying pericyclic reactions and rearrangements.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,750.00
inventory 1g
10-20 days ฿12,260.00
inventory 5g
10-20 days ฿36,660.00
inventory 10g
10-20 days ฿68,350.00
inventory 250mg
10-20 days ฿6,150.00

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1-Phenylbuta-2,3-Dien-1-One
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Used as a key intermediate in organic synthesis, particularly in the preparation of substituted allenes and heterocyclic compounds. It participates in cycloaddition reactions and metal-catalyzed couplings to build complex molecular frameworks found in bioactive molecules. Commonly employed in the development of pharmaceuticals and agrochemicals due to its reactive α,β-unsaturated ketone functionality and conjugated allene structure. Also utilized in research settings for studying pericyclic reactions and

Used as a key intermediate in organic synthesis, particularly in the preparation of substituted allenes and heterocyclic compounds. It participates in cycloaddition reactions and metal-catalyzed couplings to build complex molecular frameworks found in bioactive molecules. Commonly employed in the development of pharmaceuticals and agrochemicals due to its reactive α,β-unsaturated ketone functionality and conjugated allene structure. Also utilized in research settings for studying pericyclic reactions and rearrangements.

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