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

98%

Reagent Code: #153665
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CAS Number 900534-75-0

science Other reagents with same CAS 900534-75-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.991 g/mol
Formula C₅H₃BrF₄N₂
badge Registry Numbers
MDL Number MFCD31618520
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as a key intermediate in the synthesis of fluorinated pyrazole-based agrochemicals and pharmaceuticals. Its structure enables the introduction of highly fluorinated ethyl groups into larger molecules, enhancing metabolic stability and bioavailability. Commonly employed in the development of crop protection agents, particularly insecticides and herbicides, where fluorine substitution improves lipophilicity and target binding. Also explored in medicinal chemistry for designing bioactive compounds with improved pharmacokinetic profiles. The bromo group allows for further functionalization via cross-coupling reactions, making it a versatile building block in synthetic routes requiring fluorinated heterocycles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,520.00
inventory 250mg
10-20 days ฿3,770.00
inventory 1g
10-20 days ฿9,420.00
inventory 5g
10-20 days ฿35,680.00

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3-(1-Bromo-1,2,2,2-tetrafluoroethyl)-1H-pyrazole
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Used primarily as a key intermediate in the synthesis of fluorinated pyrazole-based agrochemicals and pharmaceuticals. Its structure enables the introduction of highly fluorinated ethyl groups into larger molecules, enhancing metabolic stability and bioavailability. Commonly employed in the development of crop protection agents, particularly insecticides and herbicides, where fluorine substitution improves lipophilicity and target binding. Also explored in medicinal chemistry for designing bioactive comp

Used primarily as a key intermediate in the synthesis of fluorinated pyrazole-based agrochemicals and pharmaceuticals. Its structure enables the introduction of highly fluorinated ethyl groups into larger molecules, enhancing metabolic stability and bioavailability. Commonly employed in the development of crop protection agents, particularly insecticides and herbicides, where fluorine substitution improves lipophilicity and target binding. Also explored in medicinal chemistry for designing bioactive compounds with improved pharmacokinetic profiles. The bromo group allows for further functionalization via cross-coupling reactions, making it a versatile building block in synthetic routes requiring fluorinated heterocycles.

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