Ethyl 6-bromoquinoline-3-carboxylate

95%

Reagent Code: #50001
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CAS Number 481054-89-1

science Other reagents with same CAS 481054-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.12 g/mol
Formula C₁₂H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD11877875
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a versatile intermediate for the preparation of more complex quinoline derivatives. Its structure allows for further functionalization, making it valuable in the development of pharmaceuticals, where quinoline-based compounds often exhibit significant biological activity. Additionally, it serves as a key building block in the synthesis of compounds with potential applications in materials science, such as organic semiconductors or light-emitting materials. The bromo and ester groups present in the molecule offer reactive sites for cross-coupling reactions, enabling the creation of diverse chemical structures for research and industrial purposes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,680.00
inventory 1g
10-20 days ฿10,008.00
inventory 100mg
10-20 days ฿2,880.00

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Ethyl 6-bromoquinoline-3-carboxylate
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This compound is primarily utilized in the field of organic synthesis, particularly as a versatile intermediate for the preparation of more complex quinoline derivatives. Its structure allows for further functionalization, making it valuable in the development of pharmaceuticals, where quinoline-based compounds often exhibit significant biological activity. Additionally, it serves as a key building block in the synthesis of compounds with potential applications in materials science, such as organic semic

This compound is primarily utilized in the field of organic synthesis, particularly as a versatile intermediate for the preparation of more complex quinoline derivatives. Its structure allows for further functionalization, making it valuable in the development of pharmaceuticals, where quinoline-based compounds often exhibit significant biological activity. Additionally, it serves as a key building block in the synthesis of compounds with potential applications in materials science, such as organic semiconductors or light-emitting materials. The bromo and ester groups present in the molecule offer reactive sites for cross-coupling reactions, enabling the creation of diverse chemical structures for research and industrial purposes.

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