2-Chloro-6,7-difluoroquinoline-3-carbaldehyde

95%

Reagent Code: #163586
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CAS Number 209909-13-7

science Other reagents with same CAS 209909-13-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.59 g/mol
Formula C₁₀H₄ClF₂NO
badge Registry Numbers
MDL Number MFCD06239276
thermostat Physical Properties
Boiling Point 344.8±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.529 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of fluorinated quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its aldehyde group allows for easy functionalization, enabling the construction of complex heterocyclic systems. Commonly employed in condensation reactions to form Schiff bases or in nucleophilic addition reactions to introduce side chains that enhance biological activity. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,920.00
inventory 250mg
10-20 days ฿3,840.00
inventory 5g
10-20 days ฿24,000.00
inventory 1g
10-20 days ฿8,000.00

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2-Chloro-6,7-difluoroquinoline-3-carbaldehyde
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Used as a key intermediate in the synthesis of fluorinated quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its aldehyde group allows for easy functionalization, enabling the construction of complex heterocyclic systems. Commonly employed in condensation reactions to form Schiff bases or in nucleophilic addition reactions to introduce side chains that enhance biological activity. Also utilized in agrochemical research for designing novel pesticides w

Used as a key intermediate in the synthesis of fluorinated quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its aldehyde group allows for easy functionalization, enabling the construction of complex heterocyclic systems. Commonly employed in condensation reactions to form Schiff bases or in nucleophilic addition reactions to introduce side chains that enhance biological activity. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles.

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