Methyl 3-iodo-1-methyl-1H-indazole-5-carboxylate

97%

Reagent Code: #210372
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CAS Number 1234616-44-4

science Other reagents with same CAS 1234616-44-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.1 g/mol
Formula C₁₀H₉IN₂O₂
badge Registry Numbers
MDL Number MFCD15071440
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. It serves as a building block for developing indazole-based molecules with potential therapeutic properties, including anti-inflammatory, anticancer, and kinase inhibitory activities. Its iodinated structure allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also utilized in the development of novel psychoactive substances, which has led to regulatory scrutiny in some regions due to misuse potential.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿530.00
inventory 1g
10-20 days ฿2,040.00
inventory 5g
10-20 days ฿10,140.00
Methyl 3-iodo-1-methyl-1H-indazole-5-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 molecules with potential therapeutic properties, including anti-inflammatory, anticancer, and kinase inhibitory activities. Its iodinated structure allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also utilized in the development of novel

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. It serves as a building block for developing indazole-based molecules with potential therapeutic properties, including anti-inflammatory, anticancer, and kinase inhibitory activities. Its iodinated structure allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also utilized in the development of novel psychoactive substances, which has led to regulatory scrutiny in some regions due to misuse potential.

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