3-(Dimethylamino)-1-(4-nitrophenyl)prop-2-en-1-one

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Reagent Code: #131009
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CAS Number 68760-11-2

science Other reagents with same CAS 68760-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.22 g/mol
Formula C₁₁H₁₂N₂O₃
badge Registry Numbers
MDL Number MFCD00121191
thermostat Physical Properties
Melting Point 151-154 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of chalcone derivatives with biological activity. It serves as a building block for compounds studied for their antimicrobial, anti-inflammatory, and anticancer properties. Commonly employed in the development of novel pharmaceuticals and in structure-activity relationship (SAR) studies due to its α,β-unsaturated ketone functionality. Also utilized in the synthesis of heterocyclic compounds such as pyrazolines and flavonoids. Its conjugated system makes it suitable for research in photophysical properties and as a ligand in coordination chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,370.00
inventory 1g
10-20 days ฿9,110.00

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3-(Dimethylamino)-1-(4-nitrophenyl)prop-2-en-1-one
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Used as an intermediate in organic synthesis, particularly in the preparation of chalcone derivatives with biological activity. It serves as a building block for compounds studied for their antimicrobial, anti-inflammatory, and anticancer properties. Commonly employed in the development of novel pharmaceuticals and in structure-activity relationship (SAR) studies due to its α,β-unsaturated ketone functionality. Also utilized in the synthesis of heterocyclic compounds such as pyrazolines and flavonoids. I

Used as an intermediate in organic synthesis, particularly in the preparation of chalcone derivatives with biological activity. It serves as a building block for compounds studied for their antimicrobial, anti-inflammatory, and anticancer properties. Commonly employed in the development of novel pharmaceuticals and in structure-activity relationship (SAR) studies due to its α,β-unsaturated ketone functionality. Also utilized in the synthesis of heterocyclic compounds such as pyrazolines and flavonoids. Its conjugated system makes it suitable for research in photophysical properties and as a ligand in coordination chemistry.

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