tert-Butyl 5-hydroxy-3-iodo-1H-indazole-1-carboxylate

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Reagent Code: #146759
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CAS Number 1426425-59-3

science Other reagents with same CAS 1426425-59-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 360.15 g/mol
Formula C₁₂H₁₃IN₂O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports derivatization for drug discovery, especially in developing anti-cancer agents. The iodine moiety allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex indazole-based molecules. Also employed in the preparation of proteolysis-targeting chimeras (PROTACs) due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,830.00
inventory 250mg
10-20 days ฿12,410.00

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tert-Butyl 5-hydroxy-3-iodo-1H-indazole-1-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports derivatization for drug discovery, especially in developing anti-cancer agents. The iodine moiety allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex indazole-based molecules. Also employed in the preparation of proteolysis-targeting chimeras (PROTACs) due to its

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports derivatization for drug discovery, especially in developing anti-cancer agents. The iodine moiety allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex indazole-based molecules. Also employed in the preparation of proteolysis-targeting chimeras (PROTACs) due to its stability and reactivity profile.

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