3-Bromo-6-nitroindazole

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Reagent Code: #145109
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CAS Number 70315-68-3

science Other reagents with same CAS 70315-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.03 g/mol
Formula C₇H₄BrN₃O₂
thermostat Physical Properties
Melting Point 235-236°C
Boiling Point 257°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted therapies. It is also employed in research settings to develop novel heterocyclic compounds with potential antitumor, antiviral, or anti-inflammatory properties. The presence of both bromo and nitro groups enables sequential reactions, facilitating the construction of complex molecular architectures in drug discovery programs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,110.00
inventory 5g
10-20 days ฿3,250.00
inventory 10g
10-20 days ฿6,070.00
inventory 50g
10-20 days ฿25,600.00
inventory 100g
10-20 days ฿48,000.00
inventory 25g
10-20 days ฿13,250.00

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3-Bromo-6-nitroindazole
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted therapies. It is also employed in research settings to develop novel heterocyclic compounds with potential antitumor, antiviral, or anti-inflammatory properties. The presence of both bromo and nitro groups enables sequential

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted therapies. It is also employed in research settings to develop novel heterocyclic compounds with potential antitumor, antiviral, or anti-inflammatory properties. The presence of both bromo and nitro groups enables sequential reactions, facilitating the construction of complex molecular architectures in drug discovery programs.

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