Ethyl 3-iodo-1H-indazole-5-carboxylate

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Reagent Code: #183503
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CAS Number 1279863-38-5

science Other reagents with same CAS 1279863-38-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.10 g/mol
Formula C₁₀H₉IN₂O₂
badge Registry Numbers
MDL Number MFCD23704369
thermostat Physical Properties
Boiling Point 427.6±25.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used as a key intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research targeting kinase inhibitors and anti-cancer agents. Its structure allows for selective modifications, making it valuable in developing compounds with activity against various diseases, including oncology and inflammatory conditions. Commonly employed in medicinal chemistry for building indazole-based scaffolds known for enhanced metabolic stability and binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,150.00
inventory 1g
10-20 days ฿3,930.00
inventory 5g
10-20 days ฿16,840.00
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Ethyl 3-iodo-1H-indazole-5-carboxylate
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Used as a key intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research targeting kinase inhibitors and anti-cancer agents. Its structure allows for selective modifications, making it valuable in developing compounds with activity against various diseases, including oncology and inflammatory conditions. Commonly employed in medicinal chemistry for building indazole-based scaffolds known for enhanced metabolic stability and binding affinity.

Used as a key intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research targeting kinase inhibitors and anti-cancer agents. Its structure allows for selective modifications, making it valuable in developing compounds with activity against various diseases, including oncology and inflammatory conditions. Commonly employed in medicinal chemistry for building indazole-based scaffolds known for enhanced metabolic stability and binding affinity.

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