tert-Butyl 5-nitro-1H-indazole-1-carboxylate

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Reagent Code: #150976
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CAS Number 129488-09-1

science Other reagents with same CAS 129488-09-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.25 g/mol
Formula C₁₂H₁₃N₃O₄
badge Registry Numbers
MDL Number MFCD07779196
thermostat Physical Properties
Boiling Point 406.1 °C(Predicted)
inventory_2 Storage & Handling
Density 1.34 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a protected indazole derivative, allowing selective functionalization at other positions of the heterocycle during multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing biologically active molecules targeting inflammatory and neurological disorders. Also utilized in the preparation of agrochemicals and functional materials due to its stability and reactivity profile in cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿690.00
inventory 1g
10-20 days ฿1,780.00
inventory 5g
10-20 days ฿6,660.00
inventory 10g
10-20 days ฿12,290.00
inventory 25g
10-20 days ฿22,500.00

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tert-Butyl 5-nitro-1H-indazole-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a protected indazole derivative, allowing selective functionalization at other positions of the heterocycle during multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing biologically active molecules targeting inflammatory and neurological disorders. Also utilized in the preparation of agrochemicals and functional ma

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a protected indazole derivative, allowing selective functionalization at other positions of the heterocycle during multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing biologically active molecules targeting inflammatory and neurological disorders. Also utilized in the preparation of agrochemicals and functional materials due to its stability and reactivity profile in cross-coupling reactions.

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