1-(p-Tolyl)butane-1,3-dione

≥98%(GC)

Reagent Code: #244492
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CAS Number 4023-79-4

science Other reagents with same CAS 4023-79-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.22 g/mol
Formula C₁₁H₁₂O₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex molecules. Commonly employed in the synthesis of heterocyclic compounds, including pyrazoles and isoxazoles, which are prevalent in bioactive molecules. Also utilized in the development of ligands for metal-catalyzed reactions. Its ketone groups participate in condensation and cyclization reactions, enabling the formation of carbon–carbon and carbon–heteroatom bonds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,890.00
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1-(p-Tolyl)butane-1,3-dione
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex molecules. Commonly employed in the synthesis of heterocyclic compounds, including pyrazoles and isoxazoles, which are prevalent in bioactive molecules. Also utilized in the development of ligands for metal-catalyzed reactions. Its ketone groups participate in condensation and cyclizatio

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex molecules. Commonly employed in the synthesis of heterocyclic compounds, including pyrazoles and isoxazoles, which are prevalent in bioactive molecules. Also utilized in the development of ligands for metal-catalyzed reactions. Its ketone groups participate in condensation and cyclization reactions, enabling the formation of carbon–carbon and carbon–heteroatom bonds.

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