N-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pivalamide

96%

Reagent Code: #218293
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CAS Number 1073354-10-5

science Other reagents with same CAS 1073354-10-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.20 g/mol
Formula C₁₇H₂₆BNO₃
badge Registry Numbers
MDL Number MFCD05663849
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl scaffolds. The pivalamide moiety acts as a directing and stabilizing group, enhancing reactivity and selectivity during transformations. Commonly employed in medicinal chemistry for late-stage functionalization of aromatic systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,990.00
5g
10-20 days ฿9,330.00
N-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pivalamide
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl scaffolds. The pivalamide moiety acts as a directing and stabilizing group, enhancing reactivity and selectivity during transformations. Commonly employed in medic

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl scaffolds. The pivalamide moiety acts as a directing and stabilizing group, enhancing reactivity and selectivity during transformations. Commonly employed in medicinal chemistry for late-stage functionalization of aromatic systems.

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