tert-Butyl 4-(difluoromethyl)piperidine-1-carboxylate

97%

Reagent Code: #151410
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CAS Number 1093759-68-2

science Other reagents with same CAS 1093759-68-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.27 g/mol
Formula C₁₁H₁₉F₂NO₂
badge Registry Numbers
MDL Number MFCD11054102
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its piperidine core with a difluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving bioavailability and blood-brain barrier penetration. Commonly employed in medicinal chemistry for optimizing lead compounds in neurodegenerative disease research and psychiatric disorder treatments. The tert-butyl carbamate (Boc) protecting group allows for selective functionalization during multi-step syntheses, enabling controlled modification of the piperidine nitrogen.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,180.00
inventory 250mg
10-20 days ฿10,500.00
inventory 1g
10-20 days ฿13,200.00

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tert-Butyl 4-(difluoromethyl)piperidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its piperidine core with a difluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving bioavailability and blood-brain barrier penetration. Commonly employed in medicinal chemistry for optimizing lead compounds in neurodegenerative disease research and psychiatric disorder treatments. The tert-butyl carbamate (Boc) pr
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its piperidine core with a difluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving bioavailability and blood-brain barrier penetration. Commonly employed in medicinal chemistry for optimizing lead compounds in neurodegenerative disease research and psychiatric disorder treatments. The tert-butyl carbamate (Boc) protecting group allows for selective functionalization during multi-step syntheses, enabling controlled modification of the piperidine nitrogen.
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