N,N-Diethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine

98%

Reagent Code: #219649
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CAS Number 1218791-45-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.17 g/mol
Formula C₁₄H₂₄BN₃O₂
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MDL Number MFCD12546555
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group readily participates in palladium-catalyzed coupling with aryl or heteroaryl halides, making it valuable for constructing complex nitrogen-containing heterocycles. Commonly employed in the development of bioactive molecules, particularly in medicinal chemistry for drug discovery and optimization. Stable and compatible with a variety of functional groups, it allows for efficient late-stage functionalization in synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,920.00
inventory 250mg
10-20 days ฿4,930.00
inventory 1g
10-20 days ฿13,140.00
N,N-Diethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group readily participates in palladium-catalyzed coupling with aryl or heteroaryl halides, making it valuable for constructing complex nitrogen-containing heterocycles. Commonly employed in the development of bioactive molecules, particularly in medicinal chemistry for drug discovery and optimization. Stable and compatible with a variety of functional groups, it allows for efficient late-stage functionalization in synthetic routes.
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