(R)-1-(4-Bromophenyl)-2,2,2-trifluoroethanamine

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Reagent Code: #230529
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CAS Number 843608-53-7

science Other reagents with same CAS 843608-53-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.05 g/mol
Formula C₈H₇BrF₃N
badge Registry Numbers
MDL Number MFCD07374594
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its trifluoromethyl and bromo-substituted aryl groups make it valuable in medicinal chemistry for enhancing metabolic stability and binding affinity. Commonly employed in asymmetric synthesis to introduce chirality in active pharmaceutical ingredients (APIs). Also utilized in the preparation of fluorinated analogs of bioactive molecules, where the fluorine atoms improve lipophilicity and bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,310.00
inventory 250mg
10-20 days ฿2,340.00
inventory 1g
10-20 days ฿8,590.00
inventory 5g
10-20 days ฿40,140.00

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(R)-1-(4-Bromophenyl)-2,2,2-trifluoroethanamine
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its trifluoromethyl and bromo-substituted aryl groups make it valuable in medicinal chemistry for enhancing metabolic stability and binding affinity. Commonly employed in asymmetric synthesis to introduce chirality in active pharmaceutical ingredients (APIs). Also utilized in the preparation of fluorinated analogs of bioactive molecules, where the fluorine atoms impro

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its trifluoromethyl and bromo-substituted aryl groups make it valuable in medicinal chemistry for enhancing metabolic stability and binding affinity. Commonly employed in asymmetric synthesis to introduce chirality in active pharmaceutical ingredients (APIs). Also utilized in the preparation of fluorinated analogs of bioactive molecules, where the fluorine atoms improve lipophilicity and bioavailability.

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