4-Bromo-5-cyclopropyl-3-(trifluoromethyl)-1H-pyrazole

≥95%

Reagent Code: #151212
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CAS Number 1057659-72-9

science Other reagents with same CAS 1057659-72-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.04 g/mol
Formula C₇H₆BrF₃N₂
badge Registry Numbers
MDL Number MFCD28991862
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of novel pesticides and fungicides. Its structure supports high biological activity, making it valuable in crop protection formulations. Also employed in medicinal chemistry for constructing bioactive molecules, especially in the design of kinase inhibitors and anti-inflammatory agents. The bromo and trifluoromethyl groups allow for further functionalization via cross-coupling reactions, enabling diverse compound libraries for screening in drug discovery.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿40,300.00

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4-Bromo-5-cyclopropyl-3-(trifluoromethyl)-1H-pyrazole
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Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of novel pesticides and fungicides. Its structure supports high biological activity, making it valuable in crop protection formulations. Also employed in medicinal chemistry for constructing bioactive molecules, especially in the design of kinase inhibitors and anti-inflammatory agents. The bromo and trifluoromethyl groups allow for further functionalization via cross-coupling reactions, enabling diverse compoun

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of novel pesticides and fungicides. Its structure supports high biological activity, making it valuable in crop protection formulations. Also employed in medicinal chemistry for constructing bioactive molecules, especially in the design of kinase inhibitors and anti-inflammatory agents. The bromo and trifluoromethyl groups allow for further functionalization via cross-coupling reactions, enabling diverse compound libraries for screening in drug discovery.

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