3-bromoquinoline-7-carboxylic acid

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Reagent Code: #144045
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CAS Number 1344046-13-4

science Other reagents with same CAS 1344046-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.07 g/mol
Formula C₁₀H₆BrNO₂
badge Registry Numbers
MDL Number MFCD20327982
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimalarial agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Also employed in research settings to develop fluorescent probes due to the quinoline core’s photophysical properties. Commonly utilized in cross-coupling reactions to build complex heterocyclic systems for drug discovery and materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,250.00
inventory 500mg
10-20 days ฿26,300.00

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3-bromoquinoline-7-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimalarial agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Also employed in research settings to develop fluorescent probes due to the quinoline core’s photophysical properties. Commonly utilized in cross-coupling reactions to build complex heterocyclic systems for drug discovery and

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimalarial agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Also employed in research settings to develop fluorescent probes due to the quinoline core’s photophysical properties. Commonly utilized in cross-coupling reactions to build complex heterocyclic systems for drug discovery and materials science.

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