Methyl3-iodo-2-methyl-2H-indazole-6-carboxylate

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Reagent Code: #213802
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CAS Number 1363382-86-8

science Other reagents with same CAS 1363382-86-8

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Weight 316.1 g/mol
Formula C₁₀H₉IN₂O₂
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MDL Number MFCD19443885
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Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. It serves as a building block for developing indazole-based drug candidates, particularly in the discovery of kinase inhibitors and anti-inflammatory agents. Its iodinated structure allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in the development of potential anticancer and neuroprotective agents due to the indazole scaffold’s biological relevance.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,420.00
inventory 250mg
10-20 days ฿19,830.00
inventory 500mg
10-20 days ฿33,010.00
inventory 1g
10-20 days ฿49,400.00

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Methyl3-iodo-2-methyl-2H-indazole-6-carboxylate
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Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. It serves as a building block for developing indazole-based drug candidates, particularly in the discovery of kinase inhibitors and anti-inflammatory agents. Its iodinated structure allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in the development of potential anticancer and neuroprote

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. It serves as a building block for developing indazole-based drug candidates, particularly in the discovery of kinase inhibitors and anti-inflammatory agents. Its iodinated structure allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in the development of potential anticancer and neuroprotective agents due to the indazole scaffold’s biological relevance.

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