4,4,4-Trifluoro-1-phenyl-1,3-butanedione

Standard for GC, ≥99.9%(GC)

Reagent Code: #238133
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CAS Number 326-06-7

science Other reagents with same CAS 326-06-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.16 g/mol
Formula C₆H₅COCH₂COCF₃
badge Registry Numbers
EC Number 206-307-8
MDL Number MFCD00000425
thermostat Physical Properties
Melting Point 38-40 °C(lit.)
Boiling Point 224 °C(lit.)
inventory_2 Storage & Handling
Density 1.113 g/cm3
Storage Room temperature

description Product Description

Widely used as a β-diketone ligand in coordination chemistry, particularly for forming stable chelate complexes with metal ions. Its electron-withdrawing trifluoromethyl group enhances the acidity of the active methylene, making it highly effective in synthesizing metal-organic frameworks and luminescent complexes. Commonly employed in the preparation of europium and terbium complexes for use in organic light-emitting diodes (OLEDs) and fluorescent sensors. Also serves as a building block in pharmaceutical and agrochemical synthesis due to its reactivity in condensation and cyclization reactions. Its stability and solubility in organic solvents make it suitable for solution-based processing in material science applications.

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inventory 1g
10-20 days ฿1,280.00

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4,4,4-Trifluoro-1-phenyl-1,3-butanedione
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Widely used as a β-diketone ligand in coordination chemistry, particularly for forming stable chelate complexes with metal ions. Its electron-withdrawing trifluoromethyl group enhances the acidity of the active methylene, making it highly effective in synthesizing metal-organic frameworks and luminescent complexes. Commonly employed in the preparation of europium and terbium complexes for use in organic light-emitting diodes (OLEDs) and fluorescent sensors. Also serves as a building block in pharmaceutic

Widely used as a β-diketone ligand in coordination chemistry, particularly for forming stable chelate complexes with metal ions. Its electron-withdrawing trifluoromethyl group enhances the acidity of the active methylene, making it highly effective in synthesizing metal-organic frameworks and luminescent complexes. Commonly employed in the preparation of europium and terbium complexes for use in organic light-emitting diodes (OLEDs) and fluorescent sensors. Also serves as a building block in pharmaceutical and agrochemical synthesis due to its reactivity in condensation and cyclization reactions. Its stability and solubility in organic solvents make it suitable for solution-based processing in material science applications.

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