tert-butyl 3-methylenepiperidine-1-carboxylate

98%

Reagent Code: #242659
label
Alias 1-Tert-butoxycarbonyl-3-methylenepiperidine
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CAS Number 276872-89-0

science Other reagents with same CAS 276872-89-0

blur_circular Chemical Specifications

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Weight 197.14 g/mol
Formula C₁₁H₁₉NO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and central nervous system agents. Its piperidine backbone with a protected amine group makes it valuable for constructing nitrogen-containing heterocycles. The methylene group allows for further functionalization via reactions such as hydrogenation, epoxidation, or cross-coupling, enabling structural diversification. Commonly employed in medicinal chemistry for lead optimization and the preparation of analogs in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿980.00
inventory 5g
10-20 days ฿4,460.00
inventory 250mg
10-20 days ฿350.00

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tert-butyl 3-methylenepiperidine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and central nervous system agents. Its piperidine backbone with a protected amine group makes it valuable for constructing nitrogen-containing heterocycles. The methylene group allows for further functionalization via reactions such as hydrogenation, epoxidation, or cross-coupling, enabling structural diversification. Commonly employed in medicinal chemistry for lead optimization and the preparation o
Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and central nervous system agents. Its piperidine backbone with a protected amine group makes it valuable for constructing nitrogen-containing heterocycles. The methylene group allows for further functionalization via reactions such as hydrogenation, epoxidation, or cross-coupling, enabling structural diversification. Commonly employed in medicinal chemistry for lead optimization and the preparation of analogs in drug discovery programs.
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