4-Bromo-7-fluoro-1H-indazole

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Reagent Code: #150266
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CAS Number 1186334-63-3

science Other reagents with same CAS 1186334-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.02 g/mol
Formula C₇H₄BrFN₂
badge Registry Numbers
MDL Number MFCD16658655
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the design of bioactive molecules with high selectivity and potency. Commonly employed in medicinal chemistry research to construct indazole-based scaffolds that modulate cellular signaling pathways. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies. Its halogen substituents allow for further functionalization via cross-coupling reactions, making it valuable in drug discovery and development.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿820.00
inventory 1g
10-20 days ฿2,260.00
inventory 5g
10-20 days ฿9,860.00
inventory 10g
10-20 days ฿19,670.00
inventory 25g
10-20 days ฿43,180.00

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4-Bromo-7-fluoro-1H-indazole
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the design of bioactive molecules with high selectivity and potency. Commonly employed in medicinal chemistry research to construct indazole-based scaffolds that modulate cellular signaling pathways. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies. Its halogen substituents allow fo

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the design of bioactive molecules with high selectivity and potency. Commonly employed in medicinal chemistry research to construct indazole-based scaffolds that modulate cellular signaling pathways. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies. Its halogen substituents allow for further functionalization via cross-coupling reactions, making it valuable in drug discovery and development.

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