N-(4-nitrobenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline

95%

Reagent Code: #218312
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CAS Number 380152-00-1

science Other reagents with same CAS 380152-00-1

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scatter_plot Molecular Information
Weight 354.20792 g/mol
Formula C₁₉H₂₃BN₂O₄
badge Registry Numbers
MDL Number MFCD22571997
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of nitrogen-containing aromatic systems for drug discovery and functional materials. Stable and compatible with a wide range of functional groups, making it valuable in multi-step organic synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,200.00
inventory 1g
10-20 days ฿46,080.00

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N-(4-nitrobenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of nitrogen-containing aromatic systems for drug discovery and functional materials. Stable and compatible with a wide range of functional groups, making it valuable in multi-step organic synthesis.

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of nitrogen-containing aromatic systems for drug discovery and functional materials. Stable and compatible with a wide range of functional groups, making it valuable in multi-step organic synthesis.

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