2-CHLORO-6-METHOXYQUINOLINE-3-CARBALDEHYDE

99%

Reagent Code: #162654
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CAS Number 73568-29-3

science Other reagents with same CAS 73568-29-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.64 g/mol
Formula C₁₁H₈ClNO₂
badge Registry Numbers
MDL Number MFCD00160585
thermostat Physical Properties
Melting Point 149-151 °C(lit.)
Boiling Point 373.9±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.348±0.06 g/cm3(Predicted)
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its aldehyde and chlorine functional groups allow for selective derivatization, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies. Also utilized in the development of fluorescent probes due to the inherent photophysical properties of the quinoline core.

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Test Parameter Specification
Appearance White to yellow to pale orange to orange to pale brown to brown powder
Purity (%) 98.5-100%
Free Acid 0-0.5%
Melting Point (°C) 145.0-151.0
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,460.00
inventory 25g
10-20 days ฿28,910.00
inventory 1g
10-20 days ฿1,880.00

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2-CHLORO-6-METHOXYQUINOLINE-3-CARBALDEHYDE
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Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its aldehyde and chlorine functional groups allow for selective derivatization, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies. Also utilized in the development of fluorescent probes due to the inherent photophysical properties of the quinoline core.

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its aldehyde and chlorine functional groups allow for selective derivatization, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies. Also utilized in the development of fluorescent probes due to the inherent photophysical properties of the quinoline core.

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