8-Hydroxy-7-propylquinoline

≥98%

Reagent Code: #195182
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CAS Number 58327-60-9

science Other reagents with same CAS 58327-60-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₁₂H₁₃NO
badge Registry Numbers
MDL Number MFCD00059755
thermostat Physical Properties
Melting Point 0°C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial drug development. Its hydroxyl and propyl functional groups allow for selective modifications, enabling the creation of derivatives with enhanced biological activity. Also employed in coordination chemistry as a ligand for metal ions, useful in catalysis and sensor design. Shows potential in materials science for developing fluorescent probes due to its ability to chelate metals and exhibit luminescent properties under UV light.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,840.00
inventory 1g
10-20 days ฿9,850.00

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8-Hydroxy-7-propylquinoline
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Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial drug development. Its hydroxyl and propyl functional groups allow for selective modifications, enabling the creation of derivatives with enhanced biological activity. Also employed in coordination chemistry as a ligand for metal ions, useful in catalysis and sensor design. Shows potential in materials science for developing fluorescent probes due to its ability to chelate metals and exhibit lumine

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial drug development. Its hydroxyl and propyl functional groups allow for selective modifications, enabling the creation of derivatives with enhanced biological activity. Also employed in coordination chemistry as a ligand for metal ions, useful in catalysis and sensor design. Shows potential in materials science for developing fluorescent probes due to its ability to chelate metals and exhibit luminescent properties under UV light.

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