Methyl 5-bromo-1H-indazole-7-carboxylate

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Reagent Code: #207070
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CAS Number 898747-24-5

science Other reagents with same CAS 898747-24-5

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Weight 255.07 g/mol
Formula C₉H₇BrN₂O₂
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Its structure supports modification for targeted drug design, especially in oncology and inflammation-related therapies. The bromo functional group allows for cross-coupling reactions, enabling the introduction of various substituents to optimize potency and selectivity. Also employed in the preparation of indazole-based small molecules for use in biochemical assays and receptor binding studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿620.00
inventory 1g
10-20 days ฿2,060.00
inventory 5g
10-20 days ฿8,960.00

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Methyl 5-bromo-1H-indazole-7-carboxylate
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Its structure supports modification for targeted drug design, especially in oncology and inflammation-related therapies. The bromo functional group allows for cross-coupling reactions, enabling the introduction of various substituents to optimize potency and selectivity. Also employed in the preparation of indazole-based small molecules for use in

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Its structure supports modification for targeted drug design, especially in oncology and inflammation-related therapies. The bromo functional group allows for cross-coupling reactions, enabling the introduction of various substituents to optimize potency and selectivity. Also employed in the preparation of indazole-based small molecules for use in biochemical assays and receptor binding studies.

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