8-Benzyloxy-5-(2-bromoacetyl)-2-hydroxyquinoline

98%

Reagent Code: #149212
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CAS Number 100331-89-3

science Other reagents with same CAS 100331-89-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.21 g/mol
Formula C₁₈H₁₄BrNO₃
badge Registry Numbers
MDL Number MFCD09025318
thermostat Physical Properties
Boiling Point 602.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.479±0.06 g/cm3
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active quinoline derivatives, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. The bromoacetyl group enables easy nucleophilic substitution, facilitating conjugation with amines or thiols in drug design. Also employed in research for developing fluorescent probes due to the inherent photophysical properties of the quinoline core.

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Test Parameter Specification
Appearance off white solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿500.00
inventory 5g
10-20 days ฿2,340.00
inventory 25g
10-20 days ฿10,980.00

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8-Benzyloxy-5-(2-bromoacetyl)-2-hydroxyquinoline
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Used as an intermediate in the synthesis of biologically active quinoline derivatives, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. The bromoacetyl group enables easy nucleophilic substitution, facilitating conjugation with amines or thiols in drug design. Also employed in research for developing fluorescent probes due to the inherent photo

Used as an intermediate in the synthesis of biologically active quinoline derivatives, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. The bromoacetyl group enables easy nucleophilic substitution, facilitating conjugation with amines or thiols in drug design. Also employed in research for developing fluorescent probes due to the inherent photophysical properties of the quinoline core.

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