(R)-2,2,2-Trifluoro-1-(3-(trifluoromethyl)phenyl)ethanamine

95%

Reagent Code: #231240
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CAS Number 1213841-80-5

science Other reagents with same CAS 1213841-80-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.15 g/mol
Formula C₉H₇F₆N
badge Registry Numbers
MDL Number MFCD07374574
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its fluorinated structure enhances metabolic stability and blood-brain barrier penetration, making it valuable in the design of antidepressants, antipsychotics, and other neuroactive drugs. The compound's stereochemistry is critical for biological activity, allowing for selective interaction with neuronal receptors and enzymes. It is also employed in the preparation of fluorinated analogs in medicinal chemistry research to improve drug potency and pharmacokinetic profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿27,030.00

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(R)-2,2,2-Trifluoro-1-(3-(trifluoromethyl)phenyl)ethanamine
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its fluorinated structure enhances metabolic stability and blood-brain barrier penetration, making it valuable in the design of antidepressants, antipsychotics, and other neuroactive drugs. The compound's stereochemistry is critical for biological activity, allowing for selective interaction with neuronal receptors and enzymes. It is also employed in the prepar

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its fluorinated structure enhances metabolic stability and blood-brain barrier penetration, making it valuable in the design of antidepressants, antipsychotics, and other neuroactive drugs. The compound's stereochemistry is critical for biological activity, allowing for selective interaction with neuronal receptors and enzymes. It is also employed in the preparation of fluorinated analogs in medicinal chemistry research to improve drug potency and pharmacokinetic profiles.

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