3-Nitro-5-(trifluoromethyl)picolinic acid

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Reagent Code: #217243
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CAS Number 1214333-19-3

science Other reagents with same CAS 1214333-19-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.11 g/mol
Formula C₇H₃F₃N₂O₄
thermostat Physical Properties
Boiling Point 325.7±42.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of complex heterocyclic compounds, making it valuable in medicinal chemistry for drug discovery. Also employed in agrochemical research for designing new active ingredients in crop protection agents due to the electron-withdrawing properties of the trifluoromethyl and nitro groups. The compound’s functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for screening in biological systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿3,000.00
inventory 250mg
10-20 days ฿10,990.00
inventory 100mg
10-20 days ฿6,380.00

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3-Nitro-5-(trifluoromethyl)picolinic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of complex heterocyclic compounds, making it valuable in medicinal chemistry for drug discovery. Also employed in agrochemical research for designing new active ingredients in crop protection agents due to the electron-withdrawing properties of the trifluoromethyl and nitro groups. The compound’s functional groups allow fo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of complex heterocyclic compounds, making it valuable in medicinal chemistry for drug discovery. Also employed in agrochemical research for designing new active ingredients in crop protection agents due to the electron-withdrawing properties of the trifluoromethyl and nitro groups. The compound’s functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for screening in biological systems.

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