2-Amino-4-(trifluoromethyl)pyridine

97%

Reagent Code: #135028
label
Alias 4-Trifluoromethyl-2-aminopyridine; 2-amino-4-trifluoromethylpyridine
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CAS Number 106447-97-6

science Other reagents with same CAS 106447-97-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.11 g/mol
Formula C₆H₅F₃N₂
badge Registry Numbers
MDL Number MFCD00077455
thermostat Physical Properties
Melting Point 70-74 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive compounds. Its structure supports the creation of herbicides and plant growth regulators due to the electron-withdrawing trifluoromethyl group enhancing stability and activity. Also employed in the preparation of kinase inhibitors and other medicinal agents where the pyridine ring acts as a scaffold for drug design. Its amino and trifluoromethyl functionalities allow for diverse chemical modifications, making it valuable in research and development of new functional materials and specialty chemicals.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿162.00
inventory 5g
10-20 days ฿880.00
inventory 25g
10-20 days ฿4,300.00

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2-Amino-4-(trifluoromethyl)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive compounds. Its structure supports the creation of herbicides and plant growth regulators due to the electron-withdrawing trifluoromethyl group enhancing stability and activity. Also employed in the preparation of kinase inhibitors and other medicinal agents where the pyridine ring acts as a scaffold for drug design. Its amino and trifluoromethyl functionalities allow for diverse

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive compounds. Its structure supports the creation of herbicides and plant growth regulators due to the electron-withdrawing trifluoromethyl group enhancing stability and activity. Also employed in the preparation of kinase inhibitors and other medicinal agents where the pyridine ring acts as a scaffold for drug design. Its amino and trifluoromethyl functionalities allow for diverse chemical modifications, making it valuable in research and development of new functional materials and specialty chemicals.

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