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

99%

Reagent Code: #242149
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CAS Number 1425970-61-1

science Other reagents with same CAS 1425970-61-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.24 g/mol
Formula C₁₇H₃₀BNO₄
badge Registry Numbers
MDL Number MFCD14706665
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Its piperidine core protected with a tert-butyloxycarbonyl (Boc) group allows for selective reactivity and stability during multi-step syntheses. It is especially valuable in the preparation of bioactive compounds where a substituted piperidine scaffold is required. The methylene linker between the boronate and the piperidine ring provides flexibility for further functionalization, making it a versatile building block in medicinal chemistry and drug development.

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Test Parameter Specification
Appearance White solid
Purity (%) 99-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿460.00
inventory 500mg
10-20 days ฿1,520.00
inventory 1g
10-20 days ฿2,990.00
inventory 5g
10-20 days ฿10,770.00

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tert-butyl 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)piperidine-1-carboxylate
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Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Its piperidine core protected with a tert-butyloxycarbonyl (Boc) group allows for selective reactivity and stability during multi-step syntheses. It is especially valuable in the preparation o

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Its piperidine core protected with a tert-butyloxycarbonyl (Boc) group allows for selective reactivity and stability during multi-step syntheses. It is especially valuable in the preparation of bioactive compounds where a substituted piperidine scaffold is required. The methylene linker between the boronate and the piperidine ring provides flexibility for further functionalization, making it a versatile building block in medicinal chemistry and drug development.

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