2-Methyl-1-phenylbutane-1,3-dione

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Reagent Code: #206506
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CAS Number 6668-24-2

science Other reagents with same CAS 6668-24-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.21 g/mol
Formula C₁₁H₁₂O₂
thermostat Physical Properties
Boiling Point 271.7°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of anticoagulant rodenticides, such as coumarin-based compounds, due to its ability to form cyclic structures upon condensation. Also employed in the production of dyes and fluorescent agents, where its keto-enol tautomerism enhances light absorption properties. Its reactivity in Michael addition and cyclization reactions makes it valuable in organic synthesis for constructing heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,710.00
inventory 250mg
10-20 days ฿3,820.00
inventory 1g
10-20 days ฿9,880.00
inventory 5g
10-20 days ฿29,650.00

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2-Methyl-1-phenylbutane-1,3-dione
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of anticoagulant rodenticides, such as coumarin-based compounds, due to its ability to form cyclic structures upon condensation. Also employed in the production of dyes and fluorescent agents, where its keto-enol tautomerism enhances light absorption properties. Its reactivity in Michael addition and cyclization reactions makes it valuable in organic synthesis for c

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of anticoagulant rodenticides, such as coumarin-based compounds, due to its ability to form cyclic structures upon condensation. Also employed in the production of dyes and fluorescent agents, where its keto-enol tautomerism enhances light absorption properties. Its reactivity in Michael addition and cyclization reactions makes it valuable in organic synthesis for constructing heterocyclic compounds.

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