[(4-Methoxyphenyl)methyl](2,2,2-trifluoroethyl)amine

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Reagent Code: #40501
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CAS Number 869472-60-6

science Other reagents with same CAS 869472-60-6

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Weight 219.2036 g/mol
Formula C₁₀H₁₂F₃NO
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MDL Number MFCD07345656
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This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a methoxyphenyl group and a trifluoroethylamine moiety, makes it a valuable intermediate for creating compounds with potential biological activity. It is often employed in the synthesis of molecules that target central nervous system disorders, due to the ability of the trifluoroethyl group to enhance binding affinity and metabolic stability. Additionally, its methoxy group can contribute to improved solubility and bioavailability of the final drug product. Researchers also explore its use in the development of herbicides and fungicides, leveraging its chemical properties to enhance efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,574.00

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[(4-Methoxyphenyl)methyl](2,2,2-trifluoroethyl)amine
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This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a methoxyphenyl group and a trifluoroethylamine moiety, makes it a valuable intermediate for creating compounds with potential biological activity. It is often employed in the synthesis of molecules that target central nervous system disorders, due to the ability of the trifluoroethyl group to enhance binding affinity and metabolic stability

This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a methoxyphenyl group and a trifluoroethylamine moiety, makes it a valuable intermediate for creating compounds with potential biological activity. It is often employed in the synthesis of molecules that target central nervous system disorders, due to the ability of the trifluoroethyl group to enhance binding affinity and metabolic stability. Additionally, its methoxy group can contribute to improved solubility and bioavailability of the final drug product. Researchers also explore its use in the development of herbicides and fungicides, leveraging its chemical properties to enhance efficacy and selectivity.

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