4-Methyl-3-(Trifluoromethyl)Benzylamine

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Reagent Code: #207817
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CAS Number 771581-64-7

science Other reagents with same CAS 771581-64-7

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scatter_plot Molecular Information
Weight 189.18 g/mol
Formula C₉H₁₀F₃N
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MDL Number MFCD06212985
inventory_2 Storage & Handling
Storage Room temperature, dryness, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for central nervous system (CNS) drugs and antidepressants. Its structure supports the creation of compounds with enhanced metabolic stability and receptor selectivity due to the presence of the trifluoromethyl group. Also employed in agrochemicals for designing herbicides and insecticides, where the amine functionality allows for easy derivatization into amides, sulfonamides, or other nitrogen-containing moieties. Its lipophilic character improves membrane permeability, making it valuable in drug design for better bioavailability.

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inventory 1g
10-20 days ฿10,790.00

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4-Methyl-3-(Trifluoromethyl)Benzylamine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for central nervous system (CNS) drugs and antidepressants. Its structure supports the creation of compounds with enhanced metabolic stability and receptor selectivity due to the presence of the trifluoromethyl group. Also employed in agrochemicals for designing herbicides and insecticides, where the amine functionality allows for easy derivatization into amides, sulfonamides, or other ni

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for central nervous system (CNS) drugs and antidepressants. Its structure supports the creation of compounds with enhanced metabolic stability and receptor selectivity due to the presence of the trifluoromethyl group. Also employed in agrochemicals for designing herbicides and insecticides, where the amine functionality allows for easy derivatization into amides, sulfonamides, or other nitrogen-containing moieties. Its lipophilic character improves membrane permeability, making it valuable in drug design for better bioavailability.

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