4-Bromo-1H-indazole-3-carboxylic acid

98%

Reagent Code: #148152
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CAS Number 885521-80-2

science Other reagents with same CAS 885521-80-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.04 g/mol
Formula C₈H₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD07367963
thermostat Physical Properties
Boiling Point 493.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry for constructing biologically active molecules targeting inflammatory diseases and neurological disorders. Its bromo and carboxylic acid functional groups allow for easy modification through cross-coupling reactions and amide formation, making it valuable in drug discovery and optimization. Also employed in the preparation of indazole-based small molecules for research in cellular signaling pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,370.00
inventory 250mg
10-20 days ฿3,220.00
inventory 1g
10-20 days ฿8,360.00
inventory 5g
10-20 days ฿41,680.00
inventory 10g
10-20 days ฿72,460.00

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4-Bromo-1H-indazole-3-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry for constructing biologically active molecules targeting inflammatory diseases and neurological disorders. Its bromo and carboxylic acid functional groups allow for easy modification through cross-coupling reactions and amide formation, making it valuable in drug discovery and optimization. Also employed in

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry for constructing biologically active molecules targeting inflammatory diseases and neurological disorders. Its bromo and carboxylic acid functional groups allow for easy modification through cross-coupling reactions and amide formation, making it valuable in drug discovery and optimization. Also employed in the preparation of indazole-based small molecules for research in cellular signaling pathways.

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