2-Amino-6-(trifluoromethyl)nicotinonitrile

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Reagent Code: #135634
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CAS Number 1026039-34-8

science Other reagents with same CAS 1026039-34-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.12 g/mol
Formula C₇H₄F₃N₃
thermostat Physical Properties
Boiling Point 271.1±40.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure supports the creation of compounds with high biological activity, making it valuable in crop protection chemistry. Also employed in research for novel heterocyclic systems due to the reactivity of the amino and nitrile groups, facilitating the formation of fused ring compounds. The trifluoromethyl group enhances metabolic stability and lipophilicity, which is beneficial in designing bioactive molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿18,280.00

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2-Amino-6-(trifluoromethyl)nicotinonitrile
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure supports the creation of compounds with high biological activity, making it valuable in crop protection chemistry. Also employed in research for novel heterocyclic systems due to the reactivity of the amino and nitrile groups, facilitating the formation of fused ring compounds. The trifluoromethyl group enhances metabolic stability and

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure supports the creation of compounds with high biological activity, making it valuable in crop protection chemistry. Also employed in research for novel heterocyclic systems due to the reactivity of the amino and nitrile groups, facilitating the formation of fused ring compounds. The trifluoromethyl group enhances metabolic stability and lipophilicity, which is beneficial in designing bioactive molecules.

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