2-(TRIFLUOROMETHYL)NICOTINONITRILE

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Reagent Code: #244880
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CAS Number 870066-15-2

science Other reagents with same CAS 870066-15-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.11 g/mol
Formula C₇H₃F₃N₂
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MDL Number MFCD08741366
inventory_2 Storage & Handling
Density 1.3437  g/mL at 25 °C
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 fluorinated heterocyclic systems, which are valuable for enhancing metabolic stability and binding affinity in active ingredients. Commonly employed in the manufacture of selective enzyme inhibitors and crop protection agents due to the electron-withdrawing properties of the trifluoromethyl and nitrile groups. Also utilized in medicinal chemistry for building blocks in the design of new drug candidates targeting central nervous system disorders and inflammatory diseases.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,360.00
inventory 100mg
10-20 days ฿2,480.00
inventory 250mg
10-20 days ฿5,410.00

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2-(TRIFLUOROMETHYL)NICOTINONITRILE
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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 fluorinated heterocyclic systems, which are valuable for enhancing metabolic stability and binding affinity in active ingredients. Commonly employed in the manufacture of selective enzyme inhibitors and crop protection agents due to the electron-withdrawing properties of the trifluoromethyl and nitrile groups. Also utilized in med

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 fluorinated heterocyclic systems, which are valuable for enhancing metabolic stability and binding affinity in active ingredients. Commonly employed in the manufacture of selective enzyme inhibitors and crop protection agents due to the electron-withdrawing properties of the trifluoromethyl and nitrile groups. Also utilized in medicinal chemistry for building blocks in the design of new drug candidates targeting central nervous system disorders and inflammatory diseases.

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