4-Bromo-5-nitro-1H-indazole

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Reagent Code: #150416
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CAS Number 1190315-72-0

science Other reagents with same CAS 1190315-72-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.03 g/mol
Formula C₇H₄BrN₃O₂
badge Registry Numbers
MDL Number MFCD12963526
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially 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 to develop compounds with potential antitumor, antimicrobial, or anti-inflammatory activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,110.00
inventory 250mg
10-20 days ฿2,080.00
inventory 1g
10-20 days ฿6,290.00
inventory 5g
10-20 days ฿28,980.00
inventory 10g
10-20 days ฿54,340.00

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4-Bromo-5-nitro-1H-indazole
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Used primarily as an intermediate in organic synthesis, especially 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 employ

Used primarily as an intermediate in organic synthesis, especially 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 to develop compounds with potential antitumor, antimicrobial, or anti-inflammatory activity.

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