6-(Trifluoromethyl)nicotinonitrile

97%

Reagent Code: #240003
label
Alias 5-Cyano-2-trifluoromethylpyridine
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CAS Number 216431-85-5

science Other reagents with same CAS 216431-85-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.11 g/mol
Formula C₇H₃F₃N₂
badge Registry Numbers
MDL Number MFCD03001347
thermostat Physical Properties
Melting Point 37-41 °C(lit.)
Boiling Point 37-40°C 0,3mm
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 molecules. Its structure supports the creation of compounds with insecticidal and herbicidal properties. The electron-withdrawing trifluoromethyl and nitrile groups enhance metabolic stability and binding affinity in active ingredients. Commonly employed in the manufacture of nicotinic receptor agonists and plant growth regulators. Also utilized in research for novel drug candidates targeting central nervous system disorders.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿400.00
inventory 5g
10-20 days ฿1,120.00
inventory 25g
10-20 days ฿5,220.00
inventory 100g
10-20 days ฿20,850.00

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6-(Trifluoromethyl)nicotinonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of compounds with insecticidal and herbicidal properties. The electron-withdrawing trifluoromethyl and nitrile groups enhance metabolic stability and binding affinity in active ingredients. Commonly employed in the manufacture of nicotinic receptor agonists and plant growth regulators. Also utilized in research for novel drug candida

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of compounds with insecticidal and herbicidal properties. The electron-withdrawing trifluoromethyl and nitrile groups enhance metabolic stability and binding affinity in active ingredients. Commonly employed in the manufacture of nicotinic receptor agonists and plant growth regulators. Also utilized in research for novel drug candidates targeting central nervous system disorders.

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