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

≥95%

Reagent Code: #148588
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CAS Number 1211583-69-5

science Other reagents with same CAS 1211583-69-5

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scatter_plot Molecular Information
Weight 265.03 g/mol
Formula C₈H₄BrF₃N₂
badge Registry Numbers
MDL Number MFCD22200789
inventory_2 Storage & Handling
Storage 2-8°C, 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 due to its ability to form stable derivatives that interact with biological targets. Commonly employed in the preparation of bioactive molecules exhibiting anti-inflammatory, antiviral, and antitumor activities. Its bromo and trifluoromethyl functional groups allow for selective cross-coupling reactions, making it valuable in structure-activity relationship (SAR) studies during drug discovery. Also utilized in agrochemical research for designing new active ingredients with enhanced metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,070.00
inventory 250mg
10-20 days ฿5,130.00
inventory 1g
10-20 days ฿20,420.00

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4-Bromo-3-(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. It serves as a building block in medicinal chemistry due to its ability to form stable derivatives that interact with biological targets. Commonly employed in the preparation of bioactive molecules exhibiting anti-inflammatory, antiviral, and antitumor activities. Its bromo and trifluoromethyl functional groups allow for selective cross-coupling reactions, ma

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 due to its ability to form stable derivatives that interact with biological targets. Commonly employed in the preparation of bioactive molecules exhibiting anti-inflammatory, antiviral, and antitumor activities. Its bromo and trifluoromethyl functional groups allow for selective cross-coupling reactions, making it valuable in structure-activity relationship (SAR) studies during drug discovery. Also utilized in agrochemical research for designing new active ingredients with enhanced metabolic stability.

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