tert-Butyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)carbamate

97%

Reagent Code: #151225
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CAS Number 1171897-39-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.19 g/mol
Formula C₁₆H₂₅BN₂O₄
badge Registry Numbers
MDL Number MFCD13195277
thermostat Physical Properties
Boiling Point 400.7±30.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas storage

description Product Description

Widely used in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing for the formation of biaryl and heteroaryl structures under mild conditions. The tert-butyl carbamate (Boc) protecting group stabilizes the amine functionality during reactions and can be easily removed later in the synthesis. This makes the compound particularly valuable in the development of nitrogen-containing drug candidates, where selective and stepwise construction of complex molecules is required. It is also employed in the preparation of functional materials and ligands for catalysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿900.00
inventory 250mg
10-20 days ฿2,000.00
inventory 1g
10-20 days ฿7,600.00
inventory 5g
10-20 days ฿34,240.00
tert-Butyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)carbamate
Widely used in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing for the formation of biaryl and heteroaryl structures under mild conditions. The tert-butyl carbamate (Boc) protecting group stabilizes the amine functionality during reactions and can be easily removed later in the synthesis. This makes the compound particularly valuable in the development of nitrogen-containing drug candidates, where selective and stepwise construction of complex molecules is required. It is also employed in the preparation of functional materials and ligands for catalysis.
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