Tert-Butyl 4-(3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)piperidine-1-carboxylate

97%

Reagent Code: #238232
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CAS Number 1092563-68-2

science Other reagents with same CAS 1092563-68-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 391.32 g/mol
Formula C₂₀H₃₄BN₃O₄
thermostat Physical Properties
Boiling Point 503.3±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.13±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable for constructing complex organic molecules. Commonly employed in the development of bioactive compounds and drug candidates, especially those involving pyrazole and piperidine scaffolds. The tert-butyl carbamate (Boc) group provides protection for the piperidine nitrogen, allowing selective reactivity and compatibility with multi-step synthetic routes. Widely applied in medicinal chemistry for lead optimization and library synthesis in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,340.00

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Tert-Butyl 4-(3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)piperidine-1-carboxylate
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Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable for constructing complex organic molecules. Commonly employed in the development of bioactive compounds and drug candidates, especially those involving pyrazole and piperidine scaffolds. The tert-butyl carbamate (Boc) group provides protection for the piperidine nitrogen, allowing selective reactivity a

Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable for constructing complex organic molecules. Commonly employed in the development of bioactive compounds and drug candidates, especially those involving pyrazole and piperidine scaffolds. The tert-butyl carbamate (Boc) group provides protection for the piperidine nitrogen, allowing selective reactivity and compatibility with multi-step synthetic routes. Widely applied in medicinal chemistry for lead optimization and library synthesis in drug discovery programs.

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