3-Iodo-6-methoxy-1-methyl-1H-indazole

98%

Reagent Code: #199758
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CAS Number 1431163-17-5

science Other reagents with same CAS 1431163-17-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.09 g/mol
Formula C₉H₉IN₂O
thermostat Physical Properties
Boiling Point 357.8±22.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis as an intermediate for pharmaceutical development, this compound serves as a building block in the preparation of biologically active molecules. Its structure supports the creation of indazole-based derivatives, which are of interest in medicinal chemistry due to their potential kinase inhibitory activity. It is also employed in research settings to develop compounds targeting neurological disorders and cancer pathways. The presence of iodine allows for further functionalization via cross-coupling reactions, making it valuable in structure-activity relationship (SAR) studies and drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,700.00
inventory 250mg
10-20 days ฿1,970.00
inventory 1g
10-20 days ฿5,640.00
inventory 5g
10-20 days ฿19,480.00

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3-Iodo-6-methoxy-1-methyl-1H-indazole
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Used primarily in organic synthesis as an intermediate for pharmaceutical development, this compound serves as a building block in the preparation of biologically active molecules. Its structure supports the creation of indazole-based derivatives, which are of interest in medicinal chemistry due to their potential kinase inhibitory activity. It is also employed in research settings to develop compounds targeting neurological disorders and cancer pathways. The presence of iodine allows for further functio

Used primarily in organic synthesis as an intermediate for pharmaceutical development, this compound serves as a building block in the preparation of biologically active molecules. Its structure supports the creation of indazole-based derivatives, which are of interest in medicinal chemistry due to their potential kinase inhibitory activity. It is also employed in research settings to develop compounds targeting neurological disorders and cancer pathways. The presence of iodine allows for further functionalization via cross-coupling reactions, making it valuable in structure-activity relationship (SAR) studies and drug discovery programs.

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