4-Bromo-5-(trifluoromethyl)-1H-indazole

≥95%

Reagent Code: #148637
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CAS Number 1428234-73-4

science Other reagents with same CAS 1428234-73-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.03 g/mol
Formula C₈H₄BrF₃N₂
badge Registry Numbers
MDL Number MFCD23713147
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. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Also employed in agrochemical research for designing novel pesticides with improved metabolic stability. The bromo and trifluoromethyl groups facilitate further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,480.00
inventory 250mg
10-20 days ฿2,480.00
inventory 1g
10-20 days ฿6,610.00
inventory 5g
10-20 days ฿25,140.00

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4-Bromo-5-(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 supports binding to specific enzyme active sites, enhancing selectivity and potency. Also employed in agrochemical research for designing novel pesticides with improved metabolic stability. The bromo and trifluoromethyl groups facilitate further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for bui

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Also employed in agrochemical research for designing novel pesticides with improved metabolic stability. The bromo and trifluoromethyl groups facilitate further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules.

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