Benzyl 3-amino-4,4-difluoropiperidine-1-carboxylate

95%

Reagent Code: #152405
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CAS Number 1207852-56-9

science Other reagents with same CAS 1207852-56-9

blur_circular Chemical Specifications

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Weight 270.28 g/mol
Formula C₁₃H₁₆F₂N₂O₂
badge Registry Numbers
MDL Number MFCD18632710
inventory_2 Storage & Handling
Storage Room temperature, sealed, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its piperidine backbone with fluorinated substituents enhances metabolic stability and blood-brain barrier penetration, making it valuable in medicinal chemistry. The benzyl carbamate group serves as a protecting group for the amine, allowing controlled deprotection during multi-step syntheses. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in research focused on neurological and psychiatric conditions.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿16,550.00
inventory 100mg
10-20 days ฿26,030.00
inventory 250mg
10-20 days ฿52,490.00

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Benzyl 3-amino-4,4-difluoropiperidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its piperidine backbone with fluorinated substituents enhances metabolic stability and blood-brain barrier penetration, making it valuable in medicinal chemistry. The benzyl carbamate group serves as a protecting group for the amine, allowing controlled deprotection during multi-step syntheses. Commonly employed in the preparation of enzy

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its piperidine backbone with fluorinated substituents enhances metabolic stability and blood-brain barrier penetration, making it valuable in medicinal chemistry. The benzyl carbamate group serves as a protecting group for the amine, allowing controlled deprotection during multi-step syntheses. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in research focused on neurological and psychiatric conditions.

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