4-Bromo-2-methyl-2H-indazole

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Reagent Code: #146601
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CAS Number 590417-93-9

science Other reagents with same CAS 590417-93-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.06 g/mol
Formula C₈H₇BrN₂
badge Registry Numbers
MDL Number MFCD09870046
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a synthetic intermediate in pharmaceutical research, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure serves as a scaffold in medicinal chemistry for designing compounds with potential anticancer, anti-inflammatory, and neuroprotective activities. The bromine atom allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification of compound libraries in drug discovery. Also investigated for its role in synthesizing selective modulators of central nervous system receptors.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿910.00
inventory 5g
10-20 days ฿4,550.00
inventory 25g
10-20 days ฿14,020.00
inventory 100g
10-20 days ฿55,310.00

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4-Bromo-2-methyl-2H-indazole
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Used primarily as a synthetic intermediate in pharmaceutical research, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure serves as a scaffold in medicinal chemistry for designing compounds with potential anticancer, anti-inflammatory, and neuroprotective activities. The bromine atom allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification of compound libraries in drug discovery. Also

Used primarily as a synthetic intermediate in pharmaceutical research, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure serves as a scaffold in medicinal chemistry for designing compounds with potential anticancer, anti-inflammatory, and neuroprotective activities. The bromine atom allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification of compound libraries in drug discovery. Also investigated for its role in synthesizing selective modulators of central nervous system receptors.

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