Ethyl 3-amino-7-bromoquinoline-2-carboxylate

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Reagent Code: #182785
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CAS Number 1260807-99-5

science Other reagents with same CAS 1260807-99-5

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Weight 295.13 g/mol
Formula C₁₂H₁₁BrN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of bioactive quinoline derivatives, particularly in pharmaceutical research targeting antimalarial and anticancer agents. Its structure serves as a key intermediate in constructing complex heterocyclic compounds. The amino and ester functional groups allow for further chemical modifications, enabling the development of compound libraries for drug discovery. Commonly employed in medicinal chemistry for building kinase inhibitors and antimicrobial agents. Also utilized in materials science for developing fluorescent probes due to the inherent photophysical properties of the quinoline core.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,500.00
inventory 100mg
10-20 days ฿2,350.00
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Ethyl 3-amino-7-bromoquinoline-2-carboxylate
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Used in the synthesis of bioactive quinoline derivatives, particularly in pharmaceutical research targeting antimalarial and anticancer agents. Its structure serves as a key intermediate in constructing complex heterocyclic compounds. The amino and ester functional groups allow for further chemical modifications, enabling the development of compound libraries for drug discovery. Commonly employed in medicinal chemistry for building kinase inhibitors and antimicrobial agents. Also utilized in materials scien
Used in the synthesis of bioactive quinoline derivatives, particularly in pharmaceutical research targeting antimalarial and anticancer agents. Its structure serves as a key intermediate in constructing complex heterocyclic compounds. The amino and ester functional groups allow for further chemical modifications, enabling the development of compound libraries for drug discovery. Commonly employed in medicinal chemistry for building kinase inhibitors and antimicrobial agents. Also utilized in materials science for developing fluorescent probes due to the inherent photophysical properties of the quinoline core.
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