1-Methyl-3-(trifluoromethyl)-1H-pyrazole-5-carbonyl chloride

95%

Reagent Code: #202945
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CAS Number 129768-24-7

science Other reagents with same CAS 129768-24-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.56 g/mol
Formula C₆H₄ClF₃N₂O
badge Registry Numbers
MDL Number MFCD03421457
thermostat Physical Properties
Boiling Point 234.2±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.56±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its reactivity allows for the introduction of the pyrazole moiety into larger molecules, enhancing biological activity. Commonly employed in coupling reactions to form amides and esters that serve as key structures in crop protection agents. Also utilized in research settings for designing novel bioactive compounds due to the stability and electronic properties imparted by the trifluoromethyl group.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,370.00
inventory 250mg
10-20 days ฿7,390.00
inventory 1g
10-20 days ฿19,900.00
1-Methyl-3-(trifluoromethyl)-1H-pyrazole-5-carbonyl chloride
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its reactivity allows for the introduction of the pyrazole moiety into larger molecules, enhancing biological activity. Commonly employed in coupling reactions to form amides and esters that serve as key structures in crop protection agents. Also utilized in research settings for designing novel bioactive compounds due to the stability and electronic properties impa

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its reactivity allows for the introduction of the pyrazole moiety into larger molecules, enhancing biological activity. Commonly employed in coupling reactions to form amides and esters that serve as key structures in crop protection agents. Also utilized in research settings for designing novel bioactive compounds due to the stability and electronic properties imparted by the trifluoromethyl group.

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