1-(2-Bromo-1,1,2,2-tetrafluoroethyl)-3,5-dimethyl-1H-pyrazole

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Reagent Code: #151441
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CAS Number 1125518-67-3

science Other reagents with same CAS 1125518-67-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.04 g/mol
Formula C₇H₇BrF₄N₂
badge Registry Numbers
MDL Number MFCD31618522
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of agrochemicals, particularly in the development of fluorinated pesticides and herbicides. Its structure supports enhanced bioavailability and stability in crop protection agents. Also explored in pharmaceutical research for building fluorinated heterocyclic compounds with potential biological activity. The bromo and tetrafluoroethyl groups allow for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry and crop science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿910.00
inventory 250mg
10-20 days ฿2,100.00
inventory 1g
10-20 days ฿6,570.00

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1-(2-Bromo-1,1,2,2-tetrafluoroethyl)-3,5-dimethyl-1H-pyrazole
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Used as an intermediate in the synthesis of agrochemicals, particularly in the development of fluorinated pesticides and herbicides. Its structure supports enhanced bioavailability and stability in crop protection agents. Also explored in pharmaceutical research for building fluorinated heterocyclic compounds with potential biological activity. The bromo and tetrafluoroethyl groups allow for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry and crop sci

Used as an intermediate in the synthesis of agrochemicals, particularly in the development of fluorinated pesticides and herbicides. Its structure supports enhanced bioavailability and stability in crop protection agents. Also explored in pharmaceutical research for building fluorinated heterocyclic compounds with potential biological activity. The bromo and tetrafluoroethyl groups allow for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry and crop science.

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