N-tert-butyl-2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]acetamide

95%

Reagent Code: #218367
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CAS Number 2056919-55-0

science Other reagents with same CAS 2056919-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.23022 g/mol
Formula C₁₈H₂₈BNO₄
badge Registry Numbers
MDL Number MFCD32206548
inventory_2 Storage & Handling
Storage 2-8°C

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 facilitates efficient coupling with aryl halides under palladium catalysis, making it valuable in the preparation of complex organic molecules, particularly in drug discovery and development. The tert-butyl amide group enhances stability and influences solubility, which can be beneficial in purification and isolation steps. Commonly employed in medicinal chemistry for constructing biaryl systems found in bioactive compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,280.00
inventory 1g
10-20 days ฿31,590.00
inventory 5g
10-20 days ฿120,000.00
N-tert-butyl-2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]acetamide
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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 facilitates efficient coupling with aryl halides under palladium catalysis, making it valuable in the preparation of complex organic molecules, particularly in drug discovery and development. The tert-butyl amide group enhances stability and influences solubility, which can be beneficial in purification and isolation st

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 facilitates efficient coupling with aryl halides under palladium catalysis, making it valuable in the preparation of complex organic molecules, particularly in drug discovery and development. The tert-butyl amide group enhances stability and influences solubility, which can be beneficial in purification and isolation steps. Commonly employed in medicinal chemistry for constructing biaryl systems found in bioactive compounds.

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