3-acetyl-6-chloroquinolin-4(1H)-one

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Reagent Code: #126347
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CAS Number 67503-73-5

science Other reagents with same CAS 67503-73-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.64 g/mol
Formula C11H8ClNO2
badge Registry Numbers
MDL Number MFCD26131199
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly those targeting antimicrobial and anti-inflammatory properties. It serves as a building block for developing quinoline derivatives, which are explored for their potential in treating infections and chronic inflammatory diseases. Additionally, it is utilized in organic chemistry studies to investigate novel reactions and pathways for creating complex heterocyclic structures. Its applications also extend to material science, where it contributes to the development of organic electronic materials due to its conjugated system.

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inventory 2g
10-20 days ฿28,240.00

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3-acetyl-6-chloroquinolin-4(1H)-one
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly those targeting antimicrobial and anti-inflammatory properties. It serves as a building block for developing quinoline derivatives, which are explored for their potential in treating infections and chronic inflammatory diseases. Additionally, it is utilized in organic chemistry studies to investigate novel reactions and pathways for creating complex heterocyclic structures. Its applications also ex

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly those targeting antimicrobial and anti-inflammatory properties. It serves as a building block for developing quinoline derivatives, which are explored for their potential in treating infections and chronic inflammatory diseases. Additionally, it is utilized in organic chemistry studies to investigate novel reactions and pathways for creating complex heterocyclic structures. Its applications also extend to material science, where it contributes to the development of organic electronic materials due to its conjugated system.

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