(3R,4S)-rel-tert-Butyl 3-amino-4-fluoropiperidine-1-carboxylate

95%

Reagent Code: #231250
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CAS Number 1273565-65-3

science Other reagents with same CAS 1273565-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.272 g/mol
Formula C₁₀H₁₉FN₂O₂
badge Registry Numbers
MDL Number MFCD18791212
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Widely used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of biologically active compounds targeting central nervous system disorders. Its structural features, including the fluorinated piperidine core and protected amine group, make it valuable in constructing potent and selective receptor modulators. Commonly employed in the preparation of antipsychotic and antidepressant drugs, where the stereochemistry and fluorine substitution enhance metabolic stability and blood-brain barrier penetration. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and ability to mimic bioactive peptide motifs.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,460.00
250mg
10-20 days ฿8,450.00
1g
10-20 days ฿29,340.00
(3R,4S)-rel-tert-Butyl 3-amino-4-fluoropiperidine-1-carboxylate
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Widely used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of biologically active compounds targeting central nervous system disorders. Its structural features, including the fluorinated piperidine core and protected amine group, make it valuable in constructing potent and selective receptor modulators. Commonly employed in the preparation of antipsychotic and antidepressant drugs, where the stereochemistry and fluorine substitution enhance metabolic stability and blood-brain barrier penetration. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and ability to mimic bioactive peptide motifs.
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