4-(Trifluoromethyl)-1H-pyrazole

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Reagent Code: #241683
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CAS Number 52222-73-8

science Other reagents with same CAS 52222-73-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 136.08 g/mol
Formula C₄H₃F₃N₂
badge Registry Numbers
MDL Number MFCD11226572
thermostat Physical Properties
Boiling Point 177.7±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to its ability to enhance metabolic stability and bioavailability. Its trifluoromethyl group contributes to increased lipophilicity and resistance to oxidative degradation, making it valuable in designing active ingredients with improved environmental persistence and efficacy. Also employed in the preparation of pyrazole-based kinase inhibitors and anti-inflammatory agents in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿700.00
inventory 1g
10-20 days ฿2,090.00
inventory 5g
10-20 days ฿9,350.00

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4-(Trifluoromethyl)-1H-pyrazole
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to its ability to enhance metabolic stability and bioavailability. Its trifluoromethyl group contributes to increased lipophilicity and resistance to oxidative degradation, making it valuable in designing active ingredients with improved environmental persistence and efficacy. Also employed in the preparation of pyrazole-based kinase inhibitors and anti-inflam

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to its ability to enhance metabolic stability and bioavailability. Its trifluoromethyl group contributes to increased lipophilicity and resistance to oxidative degradation, making it valuable in designing active ingredients with improved environmental persistence and efficacy. Also employed in the preparation of pyrazole-based kinase inhibitors and anti-inflammatory agents in medicinal chemistry research.

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