3-Bromo-6-(trifluoromethyl)-1H-indazole

98%

Reagent Code: #146339
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CAS Number 1000341-21-8

science Other reagents with same CAS 1000341-21-8

blur_circular Chemical Specifications

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Weight 265.03 g/mol
Formula C₈H₄BrF₃N₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding to enzyme active sites, making it valuable in drug discovery. Commonly employed in organic synthesis to introduce indazole motifs into larger bioactive molecules. Also utilized in agrochemical research for designing new pesticides with improved stability and activity. The bromo and trifluoromethyl groups enable further functionalization through cross-coupling reactions, enhancing its versatility in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,290.00

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3-Bromo-6-(trifluoromethyl)-1H-indazole
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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. Its structure allows for selective binding to enzyme active sites, making it valuable in drug discovery. Commonly employed in organic synthesis to introduce indazole motifs into larger bioactive molecules. Also utilized in agrochemical research for designing new pesticides with improved stability and activity. The bromo and trifluoromethyl groups enable furth

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding to enzyme active sites, making it valuable in drug discovery. Commonly employed in organic synthesis to introduce indazole motifs into larger bioactive molecules. Also utilized in agrochemical research for designing new pesticides with improved stability and activity. The bromo and trifluoromethyl groups enable further functionalization through cross-coupling reactions, enhancing its versatility in medicinal chemistry.

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