N-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

95%

Reagent Code: #215581
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CAS Number 1204742-77-7

science Other reagents with same CAS 1204742-77-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.12 g/mol
Formula C₁₄H₂₀BNO₄
badge Registry Numbers
MDL Number MFCD18383933
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions, allowing for the construction of biaryl and heterobiaryl systems. The N-methoxy amide moiety enhances stability and can act as a directing group or be further modified in multistep syntheses. Its structural features make it valuable in medicinal chemistry for building drug-like scaffolds with high functional group tolerance.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,200.00
inventory 5g
10-20 days ฿3,800.00

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N-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
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Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions, allowing for the construction of biaryl and heterobiaryl systems. The N-methoxy amide moiety enhances stability and can act as a directing group or be further modified in multistep syntheses. Its structural features make it valuable in medicinal chemistry for building drug-like scaffolds with high functional group tolerance.
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