(3S,5S)-tert-Butyl 3-amino-5-fluoropiperidine-1-carboxylate

98%

Reagent Code: #236792
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CAS Number 1932056-72-8

science Other reagents with same CAS 1932056-72-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.27 g/mol
Formula C₁₀H₁₉FN₂O₂
badge Registry Numbers
MDL Number MFCD30181025
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly pharmaceuticals targeting central nervous system disorders. Its chiral structure with defined stereochemistry makes it valuable in developing selective receptor modulators. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to the stability and functional versatility of the fluorinated piperidine scaffold. The tert-butyl carbamate (Boc) group allows for easy protection of the amine during multi-step syntheses, enabling controlled reactions in peptide-like frameworks. Widely applied in medicinal chemistry for drug discovery programs focused on improving metabolic stability and bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,480.00
inventory 250mg
10-20 days ฿14,200.00
inventory 1g
10-20 days ฿37,330.00

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(3S,5S)-tert-Butyl 3-amino-5-fluoropiperidine-1-carboxylate
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Used as a key intermediate in the synthesis of biologically active compounds, particularly pharmaceuticals targeting central nervous system disorders. Its chiral structure with defined stereochemistry makes it valuable in developing selective receptor modulators. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to the stability and functional versatility of the fluorinated piperidine scaffold. The tert-butyl carbamate (Boc) group allows for easy protection of the amin

Used as a key intermediate in the synthesis of biologically active compounds, particularly pharmaceuticals targeting central nervous system disorders. Its chiral structure with defined stereochemistry makes it valuable in developing selective receptor modulators. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to the stability and functional versatility of the fluorinated piperidine scaffold. The tert-butyl carbamate (Boc) group allows for easy protection of the amine during multi-step syntheses, enabling controlled reactions in peptide-like frameworks. Widely applied in medicinal chemistry for drug discovery programs focused on improving metabolic stability and bioavailability.

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