tert-butyl 3-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)piperidine-1-carboxylate

99%

Reagent Code: #242150
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CAS Number 2376764-47-3

science Other reagents with same CAS 2376764-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.24 g/mol
Formula C₁₇H₃₀BNO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, this compound serves as a key intermediate in the synthesis of complex organic molecules. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate-protected piperidine structure allows for selective transformations in multi-step syntheses, especially in drug discovery where nitrogen-containing heterocycles are common. After coupling, the protecting group can be easily removed under mild acidic conditions, enabling further functionalization. Its stability and reactivity profile make it a preferred building block in medicinal chemistry and process development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,860.00
inventory 500mg
10-20 days ฿18,000.00
inventory 1g
10-20 days ฿29,650.00
inventory 5g
10-20 days ฿88,950.00

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tert-butyl 3-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)piperidine-1-carboxylate
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Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, this compound serves as a key intermediate in the synthesis of complex organic molecules. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate-protected piperidine structure allows for selective transformations in multi-step syntheses, especially in drug discovery where nitrogen-containing heterocycles are common.

Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, this compound serves as a key intermediate in the synthesis of complex organic molecules. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate-protected piperidine structure allows for selective transformations in multi-step syntheses, especially in drug discovery where nitrogen-containing heterocycles are common. After coupling, the protecting group can be easily removed under mild acidic conditions, enabling further functionalization. Its stability and reactivity profile make it a preferred building block in medicinal chemistry and process development.

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