N-Methyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide

98%

Reagent Code: #219558
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CAS Number 1256359-34-8

science Other reagents with same CAS 1256359-34-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.15 g/mol
Formula C₁₅H₂₂BNO₃
badge Registry Numbers
MDL Number MFCD16660303
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its boron-containing group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and functional materials. The presence of the acetamide moiety can act as a directing group or contribute to biological activity in drug discovery intermediates. It is especially useful for constructing biaryl structures under palladium catalysis. Its stability and reactivity profile make it suitable for late-stage functionalization in complex molecule synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,630.00
inventory 250mg
10-20 days ฿4,450.00
inventory 1g
10-20 days ฿11,500.00
inventory 5g
10-20 days ฿40,250.00
N-Methyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
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Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its boron-containing group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and functional materials. The presence of the acetamide moiety can act as a directing group or contribute to biological activity in drug discovery intermediates. It is especially useful for constructing biaryl structures under palladium catalysis.

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its boron-containing group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and functional materials. The presence of the acetamide moiety can act as a directing group or contribute to biological activity in drug discovery intermediates. It is especially useful for constructing biaryl structures under palladium catalysis. Its stability and reactivity profile make it suitable for late-stage functionalization in complex molecule synthesis.

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