Tert-butyl 3-iodo-5-nitro-1H-indazole-1-carboxylate

95%

Reagent Code: #242779
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CAS Number 459133-69-8

science Other reagents with same CAS 459133-69-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 389.15 g/mol
Formula C₁₂H₁₂IN₃O₄
badge Registry Numbers
MDL Number MFCD11110274
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure allows for selective modifications, making it valuable in developing antitumor and anti-inflammatory agents. The presence of iodine facilitates cross-coupling reactions, enabling the introduction of diverse functional groups. It is also employed in the preparation of indazole-based derivatives for medicinal chemistry and drug discovery programs.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,460.00
250mg
10-20 days ฿12,360.00
500mg
10-20 days ฿20,600.00
1g
10-20 days ฿30,900.00
5g
10-20 days ฿92,680.00

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Tert-butyl 3-iodo-5-nitro-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 allows for selective modifications, making it valuable in developing antitumor and anti-inflammatory agents. The presence of iodine facilitates cross-coupling reactions, enabling the introduction of diverse functional groups. It is also employed in the preparation of indazole-based derivatives for medicinal chemistry and drug discovery programs.

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure allows for selective modifications, making it valuable in developing antitumor and anti-inflammatory agents. The presence of iodine facilitates cross-coupling reactions, enabling the introduction of diverse functional groups. It is also employed in the preparation of indazole-based derivatives for medicinal chemistry and drug discovery programs.

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