3-Iodo-6-nitro-1H-indazole

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Reagent Code: #199774
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CAS Number 70315-70-7

science Other reagents with same CAS 70315-70-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.03 g/mol
Formula C₇H₄IN₃O₂
thermostat Physical Properties
Boiling Point 458°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in heterocyclic compounds, making it valuable in the creation of bioactive molecules. The iodo and nitro groups serve as reactive sites for cross-coupling reactions and nucleophilic substitutions, enabling the construction of complex indazole derivatives. These derivatives are often explored for their potential in medicinal chemistry, including kinase inhibition and antimicrobial activity. Also employed in research settings to develop novel compounds with targeted biological properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,650.00
inventory 25g
10-20 days ฿7,280.00
inventory 100g
10-20 days ฿21,200.00

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3-Iodo-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 allows for selective functionalization in heterocyclic compounds, making it valuable in the creation of bioactive molecules. The iodo and nitro groups serve as reactive sites for cross-coupling reactions and nucleophilic substitutions, enabling the construction of complex indazole derivatives. These derivatives are often explored for their potential in medicinal chem

Used primarily as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in heterocyclic compounds, making it valuable in the creation of bioactive molecules. The iodo and nitro groups serve as reactive sites for cross-coupling reactions and nucleophilic substitutions, enabling the construction of complex indazole derivatives. These derivatives are often explored for their potential in medicinal chemistry, including kinase inhibition and antimicrobial activity. Also employed in research settings to develop novel compounds with targeted biological properties.

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