2-TRIFLUOROMETHYL-3-AMINOPYRIDINE

95%

Reagent Code: #240472
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CAS Number 106877-32-1

science Other reagents with same CAS 106877-32-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.112 g/mol
Formula C₆H₅F₃N₂
badge Registry Numbers
MDL Number MFCD09753488
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It plays a role in creating active pharmaceutical ingredients (APIs) for neurological and psychiatric disorders. Also employed in agrochemicals for the production of certain pesticides and herbicides due to its stability and reactivity. Its trifluoromethyl group enhances metabolic stability in drug design, making it valuable in medicinal chemistry for improving drug potency and bioavailability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,990.00
inventory 1g
10-20 days ฿6,150.00
inventory 5g
10-20 days ฿20,110.00

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2-TRIFLUOROMETHYL-3-AMINOPYRIDINE
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It plays a role in creating active pharmaceutical ingredients (APIs) for neurological and psychiatric disorders. Also employed in agrochemicals for the production of certain pesticides and herbicides due to its stability and reactivity. Its trifluoromethyl group enhances metabolic stability in drug design, making it valuable in medicinal chemistry for improving d

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It plays a role in creating active pharmaceutical ingredients (APIs) for neurological and psychiatric disorders. Also employed in agrochemicals for the production of certain pesticides and herbicides due to its stability and reactivity. Its trifluoromethyl group enhances metabolic stability in drug design, making it valuable in medicinal chemistry for improving drug potency and bioavailability.

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