Methyl 3-iodo-1H-indazole-6-carboxylate

95%

Reagent Code: #205510
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CAS Number 885518-82-1

science Other reagents with same CAS 885518-82-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.07 g/mol
Formula C₉H₇IN₂O₂
badge Registry Numbers
MDL Number MFCD07781616
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting cancer and inflammatory diseases. Its iodine functionality allows for further modification through cross-coupling reactions, enabling the creation of diverse compound libraries for drug discovery. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the ease of functionalization at the indazole core.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿168.00
1g
10-20 days ฿690.00
5g
10-20 days ฿1,758.00
25g
10-20 days ฿12,430.00
Methyl 3-iodo-1H-indazole-6-carboxylate
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Used primarily as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting cancer and inflammatory diseases. Its iodine functionality allows for further modification through cross-coupling reactions, enabling the creation of diverse compound libraries for drug discovery. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies

Used primarily as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting cancer and inflammatory diseases. Its iodine functionality allows for further modification through cross-coupling reactions, enabling the creation of diverse compound libraries for drug discovery. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the ease of functionalization at the indazole core.

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