N-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
98%
Reagent
Code: #220222
CAS Number
1204742-78-8
blur_circular Chemical Specifications
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Molecular Information
Weight
277.12 g/mol
Formula
C₁₄H₂₀BNO₄
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Registry Numbers
MDL Number
MFCD17015820
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Storage & Handling
Storage
Room temperature, seal, dry, inert gas
description Product Description
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. The boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of biaryl structures under mild conditions. Its N-methoxyamide moiety enhances stability and directs regioselective functionalization in complex molecule assembly. Commonly employed in medicinal chemistry for constructing drug-like molecules, especially kinase inhibitors and bioactive aromatic derivatives. Also utilized in materials science for building conjugated organic frameworks with tailored electronic properties.
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