N-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanesulfonamide
98%
Reagent
Code: #218562
CAS Number
380430-60-4
blur_circular Chemical Specifications
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Molecular Information
Weight
297.18 g/mol
Formula
C₁₃H₂₀BNO₄S
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Registry Numbers
MDL Number
MFCD02179479
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Physical Properties
Melting Point
130 - 134 ℃ - lit.
Boiling Point
417.2 ℃ at 760 mmHg
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Storage & Handling
Density
1.19 g/cm3
Storage
Room temperature
description Product Description
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-nitrogen bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in constructing complex organic molecules, especially in drug discovery and development. The sulfonamide moiety enhances stability and influences solubility, supporting its use in designing bioactive compounds.
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N-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanesulfonamide
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-nitrogen bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in constructing complex organic molecules, especially in drug discovery and development. The sulfonamide moiety enhances stability and influences solubility, supporting its use in designing bioactive compounds.
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