8-Nitro-7-quinolinecarboxaldehyde

≥98%

Reagent Code: #217684
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CAS Number 101327-87-1

science Other reagents with same CAS 101327-87-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.17 g/mol
Formula C₁₀H₆N₂O₃
thermostat Physical Properties
Melting Point 178-182°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its nitro and aldehyde functional groups allow for selective chemical modifications, enabling the construction of complex heterocyclic systems. Commonly employed in organic research for preparing fluorescent probes and sensors due to its electron-withdrawing properties and ability to form stable Schiff bases. Also utilized in coordination chemistry as a ligand precursor for metal complexes with catalytic or biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,160.00
250mg
10-20 days ฿1,980.00
1g
10-20 days ฿5,570.00
5g
10-20 days ฿24,200.00
8-Nitro-7-quinolinecarboxaldehyde
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Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its nitro and aldehyde functional groups allow for selective chemical modifications, enabling the construction of complex heterocyclic systems. Commonly employed in organic research for preparing fluorescent probes and sensors due to its electron-withdrawing properties and ability to form stable Schiff bases. Also utilized in coordination chemistry as a li

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its nitro and aldehyde functional groups allow for selective chemical modifications, enabling the construction of complex heterocyclic systems. Commonly employed in organic research for preparing fluorescent probes and sensors due to its electron-withdrawing properties and ability to form stable Schiff bases. Also utilized in coordination chemistry as a ligand precursor for metal complexes with catalytic or biological activity.

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