2-(diethylamino)-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethane-1-sulfonamide
95%
Reagent
Code: #218329
CAS Number
756520-46-4
blur_circular Chemical Specifications
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Molecular Information
Weight
382.32574 g/mol
Formula
C₁₈H₃₁BN₂O₄S
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Registry Numbers
MDL Number
MFCD22494664
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Storage & Handling
Storage
Room temperature
description Product Description
Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. The boronate ester group facilitates coupling with aryl halides under palladium catalysis, making it valuable in constructing complex aromatic systems. Its sulfonamide moiety enhances solubility and binding properties, useful in medicinal chemistry for designing bioactive molecules. Commonly employed in the synthesis of functionalized anilines and in materials science for creating conjugated systems.
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