N-(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)acetamide hydrochloride

97%

Reagent Code: #219325
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CAS Number 1150561-64-0

science Other reagents with same CAS 1150561-64-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.57 g/mol
Formula C₁₃H₂₀BClN₂O₃
badge Registry Numbers
MDL Number MFCD12026097
inventory_2 Storage & Handling
Storage 2-8°C, 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 synthesis. Its boronate ester group facilitates coupling with aryl halides under palladium catalysis, making it valuable in constructing complex heterocyclic systems found in drug molecules. The acetamide moiety acts as a directing and stabilizing group, enhancing reactivity and selectivity during coupling. Commonly applied in the development of kinase inhibitors and other bioactive compounds in medicinal chemistry research. Suitable for solid-phase and solution-phase synthesis due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,840.00
inventory 250mg
10-20 days ฿4,820.00
inventory 1g
10-20 days ฿13,000.00
N-(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)acetamide hydrochloride
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its boronate ester group facilitates coupling with aryl halides under palladium catalysis, making it valuable in constructing complex heterocyclic systems found in drug molecules. The acetamide moiety acts as a directing and stabilizing group, enhancing reactivity and selectivity during coupling. Commonly applied in the development of kinase inhibitors and othe

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its boronate ester group facilitates coupling with aryl halides under palladium catalysis, making it valuable in constructing complex heterocyclic systems found in drug molecules. The acetamide moiety acts as a directing and stabilizing group, enhancing reactivity and selectivity during coupling. Commonly applied in the development of kinase inhibitors and other bioactive compounds in medicinal chemistry research. Suitable for solid-phase and solution-phase synthesis due to its stability and reactivity profile.

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