3-Chloro-5-(trifluoromethyl)pyridazine

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Reagent Code: #129312
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CAS Number 845617-99-4

science Other reagents with same CAS 845617-99-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.53 g/mol
Formula C₅H₂ClF₃N₂
badge Registry Numbers
MDL Number MFCD20275278
thermostat Physical Properties
Boiling Point 218.2±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.504±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. Its structure supports the development of active ingredients that target specific enzymes in pests or weeds, improving selectivity and efficacy. Also explored in pharmaceutical research for building bioactive molecules due to the pyridazine core’s favorable interactions in biological systems. The electron-withdrawing groups enhance stability and influence lipophilicity, aiding in the optimization of agrochemical and drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,260.00
inventory 250mg
10-20 days ฿10,620.00

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3-Chloro-5-(trifluoromethyl)pyridazine
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Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. Its structure supports the development of active ingredients that target specific enzymes in pests or weeds, improving selectivity and efficacy. Also explored in pharmaceutical research for building bioactive molecules due to the pyridazine core’s favorable interactions in biological systems. The electron-withdrawing groups enhance stability and influence lipophilicity, aiding in the optimizat

Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. Its structure supports the development of active ingredients that target specific enzymes in pests or weeds, improving selectivity and efficacy. Also explored in pharmaceutical research for building bioactive molecules due to the pyridazine core’s favorable interactions in biological systems. The electron-withdrawing groups enhance stability and influence lipophilicity, aiding in the optimization of agrochemical and drug candidates.

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