(S)-4-(Trifluoromethyl)-2,3-dihydro-1H-inden-1-amine hydrochloride

95%

Reagent Code: #236888
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CAS Number 2514660-83-2

science Other reagents with same CAS 2514660-83-2

blur_circular Chemical Specifications

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Weight 237.65 g/mol
Formula C₁₀H₁₁ClF₃N
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for central nervous system (CNS) drugs. Its stereochemistry makes it valuable in developing enantioselective medications, including those targeting neurological and psychiatric disorders. Commonly employed in the manufacture of selective monoamine reuptake inhibitors, where the (S)-enantiomer contributes to enhanced biological activity and improved metabolic stability. Also utilized in research and development for asymmetric synthesis and catalysis due to its rigid indane backbone and functional handle for further chemical modification.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿6,280.00
inventory 100mg
10-20 days ฿8,180.00
inventory 250mg
10-20 days ฿13,630.00

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(S)-4-(Trifluoromethyl)-2,3-dihydro-1H-inden-1-amine hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for central nervous system (CNS) drugs. Its stereochemistry makes it valuable in developing enantioselective medications, including those targeting neurological and psychiatric disorders. Commonly employed in the manufacture of selective monoamine reuptake inhibitors, where the (S)-enantiomer contributes to enhanced biological activity and improved metabolic stability. Also utilized

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for central nervous system (CNS) drugs. Its stereochemistry makes it valuable in developing enantioselective medications, including those targeting neurological and psychiatric disorders. Commonly employed in the manufacture of selective monoamine reuptake inhibitors, where the (S)-enantiomer contributes to enhanced biological activity and improved metabolic stability. Also utilized in research and development for asymmetric synthesis and catalysis due to its rigid indane backbone and functional handle for further chemical modification.

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