cis-3-(Boc-amino)-4-(trifluormethyl)piperidine

95%

Reagent Code: #142217
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CAS Number 2734870-01-8

science Other reagents with same CAS 2734870-01-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.28 g/mol
Formula C₁₁H₁₉F₃N₂O₂
badge Registry Numbers
MDL Number MFCD22566226
thermostat Physical Properties
Boiling Point 307.3±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and antidepressants. Its piperidine backbone with a trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step syntheses. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical rigidity and ability to mimic bioactive conformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,160.00

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cis-3-(Boc-amino)-4-(trifluormethyl)piperidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and antidepressants. Its piperidine backbone with a trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step syntheses. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due t

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and antidepressants. Its piperidine backbone with a trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step syntheses. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical rigidity and ability to mimic bioactive conformations.

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