(S)-1-(4-(Trifluoromethyl)phenyl)ethanamine hydrochloride

95%

Reagent Code: #236243
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CAS Number 84499-78-5

science Other reagents with same CAS 84499-78-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.64 g/mol
Formula C₉H₁₁ClF₃N
badge Registry Numbers
MDL Number MFCD11035901
inventory_2 Storage & Handling
Storage Room temperature, inert atmosphere

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and antidepressants. Its enantiomeric purity makes it valuable in creating active ingredients where stereochemistry affects drug efficacy and safety. Commonly employed in asymmetric synthesis and as an intermediate in the preparation of trifluoromethyl-substituted aryl compounds, which are known for enhanced metabolic stability and bioavailability. Also utilized in research for novel bioactive molecules due to the favorable pharmacokinetic properties imparted by the trifluoromethyl group.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,160.00
inventory 1g
10-20 days ฿15,360.00
inventory 250mg
10-20 days ฿5,340.00
(S)-1-(4-(Trifluoromethyl)phenyl)ethanamine hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and antidepressants. Its enantiomeric purity makes it valuable in creating active ingredients where stereochemistry affects drug efficacy and safety. Commonly employed in asymmetric synthesis and as an intermediate in the preparation of trifluoromethyl-substituted aryl compounds, which are known for enhanced metabolic stability and bioavailability. Also utilized in r

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and antidepressants. Its enantiomeric purity makes it valuable in creating active ingredients where stereochemistry affects drug efficacy and safety. Commonly employed in asymmetric synthesis and as an intermediate in the preparation of trifluoromethyl-substituted aryl compounds, which are known for enhanced metabolic stability and bioavailability. Also utilized in research for novel bioactive molecules due to the favorable pharmacokinetic properties imparted by the trifluoromethyl group.

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