4-Bromo-6-nitro-1H-indazole

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Reagent Code: #146385
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CAS Number 885518-54-7

science Other reagents with same CAS 885518-54-7

blur_circular Chemical Specifications

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Weight 242.03 g/mol
Formula C₇H₄BrN₃O₂
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure supports the construction of complex heterocyclic systems, making it valuable in medicinal chemistry for designing kinase inhibitors and bioactive molecules. The bromo and nitro functional groups allow for further transformations via cross-coupling reactions, nucleophilic substitutions, or reductions, enabling the introduction of diverse substituents. It is also employed in research settings for the preparation of indazole-based compounds with potential biological activity, including anti-inflammatory and anticancer properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿159.50
inventory 250mg
10-20 days ฿533.50
inventory 1g
10-20 days ฿2,134.00

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4-Bromo-6-nitro-1H-indazole
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Used primarily as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure supports the construction of complex heterocyclic systems, making it valuable in medicinal chemistry for designing kinase inhibitors and bioactive molecules. The bromo and nitro functional groups allow for further transformations via cross-coupling reactions, nucleophilic substitutions, or reductions, enabling the introduction of diverse substituents. It is also empl

Used primarily as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure supports the construction of complex heterocyclic systems, making it valuable in medicinal chemistry for designing kinase inhibitors and bioactive molecules. The bromo and nitro functional groups allow for further transformations via cross-coupling reactions, nucleophilic substitutions, or reductions, enabling the introduction of diverse substituents. It is also employed in research settings for the preparation of indazole-based compounds with potential biological activity, including anti-inflammatory and anticancer properties.

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