Quinoline-8-carboxaldehyde

98%

Reagent Code: #228419
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CAS Number 38707-70-9

science Other reagents with same CAS 38707-70-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.17 g/mol
Formula C₁₀H₇NO
badge Registry Numbers
MDL Number MFCD00805837
thermostat Physical Properties
Melting Point 95-96°C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of antimalarial drugs. It serves as a building block in coordination chemistry, forming complexes with metal ions for use in catalysis and luminescent materials. Also employed in the development of fluorescent probes and sensors due to its ability to chelate metal ions and enhance optical properties. Its derivatives are explored in materials science for organic semiconductors and in medicinal chemistry for anticancer and antimicrobial agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿159.50
inventory 1g
10-20 days ฿490.00
inventory 5g
10-20 days ฿1,530.00
inventory 25g
10-20 days ฿7,130.00

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Quinoline-8-carboxaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of antimalarial drugs. It serves as a building block in coordination chemistry, forming complexes with metal ions for use in catalysis and luminescent materials. Also employed in the development of fluorescent probes and sensors due to its ability to chelate metal ions and enhance optical properties. Its derivatives are explored in materials science for organic semiconductors and in medicinal

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of antimalarial drugs. It serves as a building block in coordination chemistry, forming complexes with metal ions for use in catalysis and luminescent materials. Also employed in the development of fluorescent probes and sensors due to its ability to chelate metal ions and enhance optical properties. Its derivatives are explored in materials science for organic semiconductors and in medicinal chemistry for anticancer and antimicrobial agents.

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